Cas 155751-71-6,4-allyloxybutyl 2-<(R)-3-benzyloxytetradecanamido>-2-deoxy-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-6-O-trityl-β-D-glucopyranoside

155751-71-6

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Basic information

Product Name: 4-allyloxybutyl 2-<(R)-3-benzyloxytetradecanamido>-2-deoxy-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-6-O-trityl-β-D-glucopyranoside
Synonyms:
CAS NO:155751-71-6
Molecular Formula:
Molecular Weight: 1286.87
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: 4-allyloxybutyl 2-<(R)-3-benzyloxytetradecanamido>-2-deoxy-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-6-O-trityl-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 4-allyloxybutyl 2-<(R)-3-benzyloxytetradecanamido>-2-deoxy-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-6-O-trityl-β-D-glucopyranoside(155751-71-6)
EPA Substance Registry System: 4-allyloxybutyl 2-<(R)-3-benzyloxytetradecanamido>-2-deoxy-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-6-O-trityl-β-D-glucopyranoside(155751-71-6)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 155751-71-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155751-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,7,5 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155751-71:
(8*1)+(7*5)+(6*5)+(5*7)+(4*5)+(3*1)+(2*7)+(1*1)=146
146 % 10 = 6
So 155751-71-6 is a valid CAS Registry Number.

155751-71-6Upstream product

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155751-71-6Relevant academic research and scientific papers

New acyclic analogues of lipid A: synthesis of 4-phosphonoxybutyl and 3-phosphonoxypropyl glycosides of 2-amino-2-deoxy-D-glucose

Eustache, Jacques,Grob, Alfred,Retscher, Hannelore

, p. 251 - 268 (2007/10/02)

Several analogues of lipid A have been synthesized, in which the reducing monosaccharide moiety of the parent molecule has been replaced by an acyclic spacer.The new compounds show high endotoxic activity and are able to protect neutropenic mice against pseudomonas infection, two properties characteristic of LPS-like molecules.

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