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CAS

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13996-80-0

N-phenylacetyl-D-glucosamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13996-80-0 Structure

  • Basic information

    1. Product Name: N-phenylacetyl-D-glucosamine
    2. Synonyms: N-phenylacetyl-D-glucosamine
    3. CAS NO:13996-80-0
    4. Molecular Formula:
    5. Molecular Weight: 297.308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13996-80-0.mol
    9. Article Data: 2

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-phenylacetyl-D-glucosamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-phenylacetyl-D-glucosamine(13996-80-0)
    11. EPA Substance Registry System: N-phenylacetyl-D-glucosamine(13996-80-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 13996-80-0(Hazardous Substances Data)

13996-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13996-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,9 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13996-80:
(7*1)+(6*3)+(5*9)+(4*9)+(3*6)+(2*8)+(1*0)=140
140 % 10 = 0
So 13996-80-0 is a valid CAS Registry Number.

13996-80-0Relevant articles and documents

Palladium-catalysed asymmetric allylic alkylation using new chiral phosphinite-nitrogen ligands derived from D-glucosamine

Yonehara, Koji,Hashizume, Tomohiro,Mori, Kenji,Obe, Kouichi,Uemura, Sakae

, p. 415 - 416 (1999)

Novel phosphinite-nitrogen chiral ligands synthesized from D-glucosamine furnish a high level of enantiomeric excess (up to 96% ee] in palladium-catalysed allylic alkylation.

Palladium-catalyzed asymmetric allylic substitution reactions using new chiral phosphinite-oxazoline ligands derived from D-glucosamine

Yonehara, Koji,Hashizume, Tomohiro,Mori, Kenji,Ohe, Kouichi,Uemura, Sakae

, p. 9374 - 9380 (2007/10/03)

Novel 2-alkyl- or 2-aryl-4,5-(4,6-O-benzylidene-3-O-(diphenylphosphino)- 1,2-dideoxy-α-D-glucopyrano)-[2,1-d]-2-oxazolines (5a-f) have been prepared from D-glucosamine hydrochloride. They work effectively as chiral ligands and provide a high level of enantiomeric excess in palladium-catalyzed allylic alkylation and amination reactions. The allylic alkylation of 1,3-diphenyl-3- acetoxyprop-1-ene with dimethyl malonate proceeds smoothly in the presence of 0.25 mol % [Pd(η3C3H5)Cl]2 and the chiral ligand 5a having the smallest substituent on oxazoline at 0 °C within 6 h to furnish the highest enantiomeric excess (96% ee). The ligand 5a is also effective for the Pd- catalyzed amination of ethyl 1,3-diphenylprop-2-enyl carbonate, leading to the corresponding allylic amine in 94% ee. The full scope and limitations using ligands 5a-f in the allylic substitution reactions are described.

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