Cas 143520-23-4,(1R,2R,5R,6R)-2-Benzyloxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,7-dioxa-bicyclo[4.1.0]heptane

143520-23-4

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Basic information

Product Name: (1R,2R,5R,6R)-2-Benzyloxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,7-dioxa-bicyclo[4.1.0]heptane
Synonyms:
CAS NO:143520-23-4
Molecular Formula:
Molecular Weight: 744.882
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: (1R,2R,5R,6R)-2-Benzyloxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,7-dioxa-bicyclo[4.1.0]heptane(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,5R,6R)-2-Benzyloxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,7-dioxa-bicyclo[4.1.0]heptane(143520-23-4)
EPA Substance Registry System: (1R,2R,5R,6R)-2-Benzyloxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,7-dioxa-bicyclo[4.1.0]heptane(143520-23-4)

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: 143520-23-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143520-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,5,2 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143520-23:
(8*1)+(7*4)+(6*3)+(5*5)+(4*2)+(3*0)+(2*2)+(1*3)=94
94 % 10 = 4
So 143520-23-4 is a valid CAS Registry Number.

143520-23-4Upstream product

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143520-23-4Relevant academic research and scientific papers

An efficient construction of 1,2-trans-β-glycosidic linkages capitalizing on glycopyranosyl N,N,N',N'-tetramethylphosphoroamidates as shelf-stable glycosyl donors

Hashimoto,Yanagiya,Honda,Harada,Ikegami

, p. 3523 - 3526 (2007/10/02)

A highly stereocontrolled 1,2-trans-β-glycosidation reaction with or without neighbouring group participation has been developed by using benzyl- or benzoyl-protected glycopyranosyl N,N,N',N'-tetramethylphosphoramidates as shelf-stable glycosyl donors in

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