Cas 1404311-99-4,L-threonine N-[(1,1-dimethylethoxy)carbonyl]-O-(6-O-benzyl-2,3-dideoxy-β-D-threo-hex-2-enopyranosyl) methyl ester

1404311-99-4

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Basic information

Product Name: L-threonine N-[(1,1-dimethylethoxy)carbonyl]-O-(6-O-benzyl-2,3-dideoxy-β-D-threo-hex-2-enopyranosyl) methyl ester
Synonyms:
CAS NO:1404311-99-4
Molecular Formula:
Molecular Weight: 451.517
EINECS: N/A
Product Categories: N/A
Mol File: 1404311-99-4.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: L-threonine N-[(1,1-dimethylethoxy)carbonyl]-O-(6-O-benzyl-2,3-dideoxy-β-D-threo-hex-2-enopyranosyl) methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: L-threonine N-[(1,1-dimethylethoxy)carbonyl]-O-(6-O-benzyl-2,3-dideoxy-β-D-threo-hex-2-enopyranosyl) methyl ester(1404311-99-4)
EPA Substance Registry System: L-threonine N-[(1,1-dimethylethoxy)carbonyl]-O-(6-O-benzyl-2,3-dideoxy-β-D-threo-hex-2-enopyranosyl) methyl ester(1404311-99-4)

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: 1404311-99-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1404311-99-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,4,3,1 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1404311-99:
(9*1)+(8*4)+(7*0)+(6*4)+(5*3)+(4*1)+(3*1)+(2*9)+(1*9)=114
114 % 10 = 4
So 1404311-99-4 is a valid CAS Registry Number.

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1404311-99-4Relevant articles and documents

Palladium-catalyzed improved regio- and stereoselective O-glycosylation of D-glucal-derived β- And α-vinyl oxiranes

Reddy, Y. Suman,Lahiri, Rima,Vankar, Yashwant D.

, p. 4751 - 4761 (2012/10/08)

A Pd0-catalyzed glycosylation of D-glucal-derived vinyloxiranes as excellent glycosyl donors has been accomplished in a regio- and stereoselective manner. Various glycosyl acceptors upon reaction with vinyl oxiranes 1a and 1b produced the corre

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