Cas 874892-75-8,(2R,3S,4R)-2,3,4-tri-O-benzyl-1-O-(tolyl-4-sulfonyl)hept-6-yne-1,2,3,4-tetrol

874892-75-8

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Basic information

Product Name: (2R,3S,4R)-2,3,4-tri-O-benzyl-1-O-(tolyl-4-sulfonyl)hept-6-yne-1,2,3,4-tetrol
Synonyms: (2R,3S,4R)-2,3,4-tri-O-benzyl-1-O-(tolyl-4-sulfonyl)hept-6-yne-1,2,3,4-tetrol
CAS NO:874892-75-8
Molecular Formula:
Molecular Weight: 584.733
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: (2R,3S,4R)-2,3,4-tri-O-benzyl-1-O-(tolyl-4-sulfonyl)hept-6-yne-1,2,3,4-tetrol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,4R)-2,3,4-tri-O-benzyl-1-O-(tolyl-4-sulfonyl)hept-6-yne-1,2,3,4-tetrol(874892-75-8)
EPA Substance Registry System: (2R,3S,4R)-2,3,4-tri-O-benzyl-1-O-(tolyl-4-sulfonyl)hept-6-yne-1,2,3,4-tetrol(874892-75-8)

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: 874892-75-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 874892-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,8,9 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 874892-75:
(8*8)+(7*7)+(6*4)+(5*8)+(4*9)+(3*2)+(2*7)+(1*5)=238
238 % 10 = 8
So 874892-75-8 is a valid CAS Registry Number.

874892-75-8Upstream product

874892-75-8Downstream Products

874892-75-8Relevant academic research and scientific papers

Efficient synthesis of 1,2,3-triazole-fused bicyclic compounds from aldoses

Dolhem, Franck,Al Tahli, Fathia,Lievre, Catherine,Demailly, Gilles

, p. 5019 - 5023 (2005)

We would like to report an expedient synthesis of 1,2,3-triazole-fused bicyclic compounds starting from naturally occurring carbohydrates. These imino sugars were prepared in four steps from glyco-ynitols, readily available from monosaccharides. The title

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