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5239-09-8

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5239-09-8 Usage

Description

6-O-(2-O,3-O,4-O-Triacetyl-6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranose tetraacetate is a complex carbohydrate derivative with a unique structure, featuring a β-D-glucopyranose core with a 6-deoxy-α-L-mannopyranosyl moiety attached at the 6th position. This molecule is characterized by the presence of four acetyl groups and a triacetyl group on the mannopyranosyl unit, which may contribute to its potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
6-O-(2-O,3-O,4-O-Triacetyl-6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranose tetraacetate is used as an intermediate in the synthesis of various bioactive compounds, such as Isorhoifolin (I819700), a naturally occurring flavonoid with potential antidiabetic, antihyperlipidemic, and antioxidant effects. Its unique structural features make it a valuable building block for the development of novel therapeutic agents.
Used in Chemical Synthesis:
In the field of organic chemistry, 6-O-(2-O,3-O,4-O-Triacetyl-6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranose tetraacetate can be utilized as a key intermediate for the synthesis of complex carbohydrate structures and other biologically relevant molecules. Its versatile structure allows for further functionalization and modification, enabling the creation of a wide range of compounds with potential applications in various industries.
Used in Research and Development:
This molecule can also be employed in research and development settings, where it may be used to study the interactions between carbohydrates and other biomolecules, such as proteins and lipids. Understanding these interactions can provide valuable insights into the role of carbohydrates in biological processes and may lead to the discovery of new therapeutic targets and strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 5239-09-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,3 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5239-09:
(6*5)+(5*2)+(4*3)+(3*9)+(2*0)+(1*9)=88
88 % 10 = 8
So 5239-09-8 is a valid CAS Registry Number.

5239-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Neryl 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-6-O-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names hepta-O-acetyl-

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:5239-09-8 SDS

5239-09-8Relevant articles and documents

Synthesis and antiglycation activity of kaempferol-3-o- rutinoside(Nicotiflorin)

Shyaula, Sajan Lal,Abbas, Ghulam,Siddiqui, Hina,Sattar, Samina A.,Choudhary, M. Iqbal,Basha, Fatima Z.

experimental part, p. 415 - 420 (2012/09/05)

Kaempferol-3-O-α-L-rhamanopyranosyl-(1″-6″) -β-D-glucopyranoside (1) (Nicotiflorin or kaempferol-3-Orutinoside), isolated from the aerial parts of Osyris wightiana Wall. ex Wight, has exhibited a potent antiglycation activity in vitro. A short and efficient route to kaempferol-3-O-rutinoside (1) is also described in this paper. To study the Structure-Activity Relationship (SAR), few other derivatives of kaempferol were also evaluated for their antiglycation activity. Moreover the cytotoxicity analysis was also performed for these compounds prepared and SAR studies showed that sugar derivatives of kaempferol possess a promising antiglycation activity.

SYNTHESIS OF 1,2-trans-DISACCHARIDES via SUGAR THIO-ORTHOESTERS

Backinowsky, Leon V.,Tsvetkov, Yury E.,Balan, Nikolay F.,Byramova, Narguiz E.,Kochetkov, Nikolay K.

, p. 209 - 222 (2007/10/02)

The reaction of sugar 1,2-thio-orthoesters in the D-gluco, D-galacto, D-manno, and L-rhamno series with primary and secondary trityl ethers of monosaccharides, in the presence of triphenylmethylium perchlorate as catalyst, affords, stereospecifically, derivatives of 1,2-trans-disaccharides in good yields. 4-Trityl ethers of benzyl 2-acetamido-3,6-di-O-acetyl-2-deoxy-α-D-glucopyranoside and methyl 2,3,6-tri-O-benzoyl-α-D-galactopyranoside exhibit low reactivity in glycosylation by thio-ortho-esters.A reaction scheme for the glycosylation is discussed.

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