Cas 1333393-52-4,6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-1-D-galactopyranosyl Nα-(fluoren-9-ylmethoxycarbonyl)-L-serine methyl ester

1333393-52-4

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Basic information

Product Name: 6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-1-D-galactopyranosyl Nα-(fluoren-9-ylmethoxycarbonyl)-L-serine methyl ester
Synonyms:
CAS NO:1333393-52-4
Molecular Formula:
Molecular Weight: 750.805
EINECS: N/A
Product Categories: N/A
Mol File: 1333393-52-4.mol
Article Data: 1

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: 6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-1-D-galactopyranosyl Nα-(fluoren-9-ylmethoxycarbonyl)-L-serine methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-1-D-galactopyranosyl Nα-(fluoren-9-ylmethoxycarbonyl)-L-serine methyl ester(1333393-52-4)
EPA Substance Registry System: 6-O-acetyl-2-azido-3,4-di-O-benzyl-2-deoxy-1-D-galactopyranosyl Nα-(fluoren-9-ylmethoxycarbonyl)-L-serine methyl ester(1333393-52-4)

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: 1333393-52-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333393-52-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,3,9 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1333393-52:
(9*1)+(8*3)+(7*3)+(6*3)+(5*3)+(4*9)+(3*3)+(2*5)+(1*2)=144
144 % 10 = 4
So 1333393-52-4 is a valid CAS Registry Number.

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1333393-52-4Relevant articles and documents

Dimethylformamide: An unusual glycosylation modulator

Lu, Shao-Ru,Lai, Yen-Hsun,Chen, Jiun-Han,Liu, Chih-Yueh,Mong, Kwok-Kong Tony

supporting information; experimental part, p. 7315 - 7320 (2011/10/04)

A simple solution: When N,N-dimethylformamide was used to direct the stereochemical course of glycosylation reactions, 1,2-cis glycosylation products were formed with excellent selectivity. A straightforward highly α-stereoselective glycosylation involvin

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