Cas 167013-79-8,allyl 2-acetylamino-2-deoxy-3,4-dibenzyl-6-O-(2-O-acetyl-3,4-O-dibenzyl-α-L-rhamnopyranosyl)-α-D-glucopyranoside

167013-79-8

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Basic information

Product Name: allyl 2-acetylamino-2-deoxy-3,4-dibenzyl-6-O-(2-O-acetyl-3,4-O-dibenzyl-α-L-rhamnopyranosyl)-α-D-glucopyranoside
Synonyms: allyl 2-acetylamino-2-deoxy-3,4-dibenzyl-6-O-(2-O-acetyl-3,4-O-dibenzyl-α-L-rhamnopyranosyl)-α-D-glucopyranoside
CAS NO:167013-79-8
Molecular Formula:
Molecular Weight: 809.954
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: allyl 2-acetylamino-2-deoxy-3,4-dibenzyl-6-O-(2-O-acetyl-3,4-O-dibenzyl-α-L-rhamnopyranosyl)-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: allyl 2-acetylamino-2-deoxy-3,4-dibenzyl-6-O-(2-O-acetyl-3,4-O-dibenzyl-α-L-rhamnopyranosyl)-α-D-glucopyranoside(167013-79-8)
EPA Substance Registry System: allyl 2-acetylamino-2-deoxy-3,4-dibenzyl-6-O-(2-O-acetyl-3,4-O-dibenzyl-α-L-rhamnopyranosyl)-α-D-glucopyranoside(167013-79-8)

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: 167013-79-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 167013-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,0,1 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 167013-79:
(8*1)+(7*6)+(6*7)+(5*0)+(4*1)+(3*3)+(2*7)+(1*9)=128
128 % 10 = 8
So 167013-79-8 is a valid CAS Registry Number.

167013-79-8Upstream product

167013-79-8Downstream Products

167013-80-1 allyl 2-acetylamino-2-deoxy-3,4-dibenzyl-6-O-(3,4-O-dibenzyl-α-L-rhamnopyranosyl)-α-D-glucopyranoside

167013-79-8Relevant academic research and scientific papers

Studies on carbohydrates XVIII. Synthesis of tetrasaccharide corresponding to biological repeat units of Serratia marcescens O18 polysaccharide

Zhang,Mao,Chen,Cai

, p. 2283 - 2290 (1994)

The synthesis of a blocked tetrasaccharide portion of the biological repeat unit, [→2)L-Rhapα(1→2)L-Rhapα(1→2)L-Rhapα(1→6)D-GlcNAcpα(1→], of the Serratia marcescens O18 polysaccharide was described. The key intermediate compounds was 3,4-blocked -L-rhamno

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