Cas 757957-13-4,2-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosylthio)-5-benzyl-1,3,4-oxadiazole

757957-13-4

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Basic information

Product Name: 2-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosylthio)-5-benzyl-1,3,4-oxadiazole
Synonyms: 2-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosylthio)-5-benzyl-1,3,4-oxadiazole
CAS NO:757957-13-4
Molecular Formula:
Molecular Weight: 521.548
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosylthio)-5-benzyl-1,3,4-oxadiazole(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosylthio)-5-benzyl-1,3,4-oxadiazole(757957-13-4)
EPA Substance Registry System: 2-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosylthio)-5-benzyl-1,3,4-oxadiazole(757957-13-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 757957-13-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 757957-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,7,9,5 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 757957-13:
(8*7)+(7*5)+(6*7)+(5*9)+(4*5)+(3*7)+(2*1)+(1*3)=224
224 % 10 = 4
So 757957-13-4 is a valid CAS Registry Number.

757957-13-4Upstream product

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757957-13-4Relevant academic research and scientific papers

A synthesis of heteroaromatic S- and N-β-glycosides of N-acetylglucosamine under phase-transfer conditions

Kur'yanov,Chupakhina,Zemlyakov,Chirva,Shishkin,Shishkina,Kotlyar,Kamalov

, p. 460 - 466 (2005)

The use of crown ethers for a phase transfer-catalyzed synthesis of heteroaromatic glycosides of N-acetylglucosamine was studied. The solid-liquid system and catalysis by 15-crown-5 were found to provide for both the 100% conversion of α-D-glucosaminyl ch

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