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79791-38-1

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  • China Biggest Factory & Manufacturer supply Dodecylbenzenesulfonyl azide CAS: 79791-38-1

    Cas No: 79791-38-1

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79791-38-1 Usage

Description

Dodecylbenzenesulfonyl azide is a chemical compound with the formula C18H29N3O2S. It is a derivative of benzenesulfonamide, featuring a dodecyl chain and an azide functional group. Dodecylbenzenesulfonyl azide is known for its reactivity and is commonly used in various chemical synthesis processes.

Uses

1. Used in Pharmaceutical Industry:
Dodecylbenzenesulfonyl azide is used as a reactant or reagent for the synthesis of positron emission tomography (PET) ligands, specifically for imaging metabotropic glutamate receptor type 1. This application aids in the detection and monitoring of neurological disorders.
2. Used in Organic Synthesis:
Dodecylbenzenesulfonyl azide serves as a stitching agent for the introduction of aziridines into functionalized organic molecules. This process is crucial in the development of complex organic compounds and materials.
3. Used in Antibiotic Production:
In the pharmaceutical industry, dodecylbenzenesulfonyl azide is utilized as a parenteral cephalosporin, which is a type of antibiotic. It plays a vital role in the treatment of bacterial infections.
4. Used in Chemical Research:
Dodecylbenzenesulfonyl azide is employed as a reagent for intermolecular metal-catalyzed carbenoid cyclopropanations. This reaction is essential in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.
5. Used in Solid-phase Synthesis:
In the field of chemical research, dodecylbenzenesulfonyl azide is used in the solid-phase synthesis of indolecarboxylates using palladium-catalyzed reactions. This method is significant for the production of indole-based compounds, which have applications in pharmaceuticals, agrochemicals, and materials science.
6. Used in Rhodium Carbenoid N-H Insertion Reactions:
Dodecylbenzenesulfonyl azide is also used as a reagent in solid-phase rhodium carbenoid N-H insertion reactions. This reaction is crucial for the synthesis of various nitrogen-containing organic compounds, which are valuable in the development of new drugs and other chemical products.
7. Used as a Diazo-transfer Reagent:
Dodecylbenzenesulfonyl azide is utilized as a diazo-transfer reagent for activated methylene groups. This application is essential in the synthesis of various organic compounds, particularly those with complex structures.

Preparation

prepared by addition of granular sodium azide (1.3 equiv) to a mixture of isomeric sulfonyl chlorides (from a commercial mixture of isomers of p-dodecylbenzenesulfonic acid) in acetone solution.

Reactions

Reagent for Diazo-function Transfer. The title reagent has been called a safer diazo-transfer reagent, and is a mixture of 12 or more isomeric p-dodecylbenzenesulfonyl azides, ranging by HPLC from 24% to 1% in area and giving essentially a single spot by TLC. The title reagent has been shown to be very useful for the synthesis of various crystalline diazocarbonyl compounds such as diazobarbituric and diazoisopropylidenemalonic acids, derivatives and homologs of diazoacetoacetic acid, and 9-diazoanthrone (eq 1). Formation of noncrystalline byproduct dodecylsulfonamides facilitates the workup procedure and isolation of the target crys- talline diazo compounds from the reaction mixture.

storage

Dodecylbenzenesulfonyl azide is the safest of the usual are nesulfonyl azides (tosyl azide, etc.) employed in diazo-transfer processes;appropriate care should be taken,as with all azides. Use in a fume hood.

Purification Methods

elution through short column containing silica gel G with methylene chloride-hexane (1:4) as eluant.

Check Digit Verification of cas no

The CAS Registry Mumber 79791-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,9 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79791-38:
(7*7)+(6*9)+(5*7)+(4*9)+(3*1)+(2*3)+(1*8)=191
191 % 10 = 1
So 79791-38-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H29N3O2S/c1-2-3-4-5-6-7-8-9-10-11-14-17-15-12-13-16-18(17)24(22,23)21-20-19/h12-13,15-16H,2-11,14H2,1H3

79791-38-1 Well-known Company Product Price

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  • TCI America

  • (D2580)  Dodecylbenzenesulfonyl Azide (soft type) (mixture)  

  • 79791-38-1

  • 25g

  • 820.00CNY

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  • Aldrich

  • (722154)  4-Dodecylbenzenesulfonylazide  (soft type) (mixture)

  • 79791-38-1

  • 722154-25G

  • 652.86CNY

  • Detail
  • Aldrich

  • (722154)  4-Dodecylbenzenesulfonylazide  (soft type) (mixture)

  • 79791-38-1

  • 722154-100G

  • 2,490.93CNY

  • Detail

79791-38-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Dodecylbenzenesulfonyl Azide

1.2 Other means of identification

Product number -
Other names N-diazo-2-dodecylbenzenesulfonamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79791-38-1 SDS

79791-38-1Synthetic route

p-dodecylbenzenesulfonyl chloride
52499-14-6

p-dodecylbenzenesulfonyl chloride

4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

Conditions
ConditionsYield
With sodium azide In water; acetone at 10 - 30℃; Temperature; Flow reactor;82.2%
With sodium azide In water; acetone at 20℃; for 11h;
4-nitrobenzyl chloride
619-73-8

4-nitrobenzyl chloride

4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

acetoacetic acid methyl ester
105-45-3

acetoacetic acid methyl ester

4-nitrobenzyl 2-diazo-3-oxo-butanoate
82551-63-1

4-nitrobenzyl 2-diazo-3-oxo-butanoate

Conditions
ConditionsYield
With triethylamine In toluene95%
(E)-diethyl glutaconate
73178-43-5

(E)-diethyl glutaconate

4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

diethyl (E)-4-diazopent-2-enedioate
104525-94-2

diethyl (E)-4-diazopent-2-enedioate

Conditions
ConditionsYield
With triethylamine94%
methyl 3-oxohept-6-enoate
30414-57-4

methyl 3-oxohept-6-enoate

N-(tert-butoxycarbonyl)-1,4-phenylenediamine
71026-66-9

N-(tert-butoxycarbonyl)-1,4-phenylenediamine

4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

butyl 5-(3-buten-1-yl)-1-{4-[(tert-butoxycarbonyl)amino]phenyl}-1H-1,2,3-triazole-4-carboxylate
912838-01-8

butyl 5-(3-buten-1-yl)-1-{4-[(tert-butoxycarbonyl)amino]phenyl}-1H-1,2,3-triazole-4-carboxylate

Conditions
ConditionsYield
Stage #1: methyl 3-oxohept-6-enoate; N-(tert-butoxycarbonyl)-1,4-phenylenediamine; butan-1-ol With sulfuric acid for 6h; Heating / reflux;
Stage #2: 4-dodecylbenzenesulphonyl azide With triethylamine In acetonitrile at 20℃; for 6h; Heating / reflux;
Stage #3: With sodium nitrite In water; acetonitrile at 20℃;
86%
4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

cis-β,4-dioxo-3-[(phenoxyacetyl)amino]-2-azetidinepentanoic acid, (4-nitrophenyl)methyl ester
124831-38-5

cis-β,4-dioxo-3-[(phenoxyacetyl)amino]-2-azetidinepentanoic acid, (4-nitrophenyl)methyl ester

cis-α-diazo-β,4-dioxo-3-[(phenoxyacetyl)amino]-2-azetidinepentanoic acid, (4-nitrophenyl)methyl ester
119892-48-7

cis-α-diazo-β,4-dioxo-3-[(phenoxyacetyl)amino]-2-azetidinepentanoic acid, (4-nitrophenyl)methyl ester

Conditions
ConditionsYield
With triethylamine In n-heptane; dichloromethane85%
7,8-benzoquinoline
230-27-3

7,8-benzoquinoline

4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

N-(benzo[h]quinolin-10-yl)-4-dodecylbenzenesulfonamide

N-(benzo[h]quinolin-10-yl)-4-dodecylbenzenesulfonamide

Conditions
ConditionsYield
With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer In 1,2-dichloro-ethane at 20 - 80℃; for 12.1667h; Inert atmosphere;77%
4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

(E)-2-methylcyclohexanone O-methyl oxime

(E)-2-methylcyclohexanone O-methyl oxime

A

(Z)-4-dodecyl-N-[(2-(methoxyimino)cyclohexyl)methyl]benzenesulfonamide
1575700-96-7

(Z)-4-dodecyl-N-[(2-(methoxyimino)cyclohexyl)methyl]benzenesulfonamide

B

(E)-4-dodecyl-N-[(2-(methoxyimino)cyclohexyl)methyl]benzenesulfonamide
1575700-94-5

(E)-4-dodecyl-N-[(2-(methoxyimino)cyclohexyl)methyl]benzenesulfonamide

Conditions
ConditionsYield
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; silver(I) acetate; silver(I) triflimide In 1,2-dichloro-ethane at 80℃; for 24h;A 75%
B n/a
dibenzofuran
132-64-9

dibenzofuran

4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

4-azidodibenzo[b,d]furan
1399050-09-9

4-azidodibenzo[b,d]furan

Conditions
ConditionsYield
Stage #1: dibenzofuran With n-butyllithium In tetrahydrofuran at 20℃; Cooling with acetone-dry ice; Inert atmosphere;
Stage #2: 4-dodecylbenzenesulphonyl azide In tetrahydrofuran at 20℃; for 3h; Cooling with acetone-dry ice;
55%
With n-butyllithium In tetrahydrofuran
4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

(3S,4R)-3-[(R)-1-hydroxyethyl]-4-[3-(4-nitrobenzyl)-oxycarbonyl-2-oxopropyl]azetidin-2-one
75321-07-2

(3S,4R)-3-[(R)-1-hydroxyethyl]-4-[3-(4-nitrobenzyl)-oxycarbonyl-2-oxopropyl]azetidin-2-one

(3S,4R)-3-[(R)-1-hydroxyethyl)-4-[3-(4-nitrobenzyl)oxycarbonyl-2-oxo-3-diazopropyl]azetidin-2-one
74288-39-4

(3S,4R)-3-[(R)-1-hydroxyethyl)-4-[3-(4-nitrobenzyl)oxycarbonyl-2-oxo-3-diazopropyl]azetidin-2-one

Conditions
ConditionsYield
With triethylamine In acetonitrile
7-(cyclohexylmethyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine

7-(cyclohexylmethyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine

4-dodecylbenzenesulphonyl azide
79791-38-1

4-dodecylbenzenesulphonyl azide

3-azido-7-(cyclohexylmethyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine

3-azido-7-(cyclohexylmethyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine

Conditions
ConditionsYield
Stage #1: 7-(cyclohexylmethyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere;
Stage #2: 4-dodecylbenzenesulphonyl azide In tetrahydrofuran; hexane at 20℃; for 2h;
0.55 g

79791-38-1Relevant articles and documents

Microchannel synthesis method of aryl sulfonyl azide

-

Paragraph 0031-0032, (2019/07/04)

The invention discloses a microchannel synthesis method of aryl sulfonyl azide. Sodium azide and water are uniformly stirred and prepared into a material A, aryl sulfonyl chloride and acetone are uniformly stirred and prepared into a material B, and the material A and the material B are continuously fed into a microchannel reactor at the flow rate of 6mL/min-70mL/min and efficiently react to prepare the aryl sulfonyl azide. Compared with the prior art, the microchannel synthesis method has the advantages that process route operation is safe, conversion rate is high, cost is saved, and the yield of the aryl sulfonyl azide is higher than 80%.

2-thiosubstituted carbapenems

-

, (2008/06/13)

Carbapenem antibiotic compounds of the general formula: STR1 wherein the moiety STR2 is a 4, 5 or 6 membered mono, di- or tri- substituted oxygen or sulfur containing ring; wherein Z is oxygen, sulfur, sulfoxide and sulfone, pharmaceutical compositions thereof useful for the treatment of bacterial infections, processes for preparing the compounds and new intermediates useful in the process.

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