Cas 95673-09-9,Acetic acid (R)-1-((3E,7E)-(1R,2S)-2-hydroxy-1-hydroxymethyl-8-methyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester

95673-09-9

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Basic information

Product Name: Acetic acid (R)-1-((3E,7E)-(1R,2S)-2-hydroxy-1-hydroxymethyl-8-methyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester
Synonyms: Acetic acid (R)-1-((3E,7E)-(1R,2S)-2-hydroxy-1-hydroxymethyl-8-methyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester
CAS NO:95673-09-9
Molecular Formula:
Molecular Weight: 607.959
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: Acetic acid (R)-1-((3E,7E)-(1R,2S)-2-hydroxy-1-hydroxymethyl-8-methyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (R)-1-((3E,7E)-(1R,2S)-2-hydroxy-1-hydroxymethyl-8-methyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester(95673-09-9)
EPA Substance Registry System: Acetic acid (R)-1-((3E,7E)-(1R,2S)-2-hydroxy-1-hydroxymethyl-8-methyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester(95673-09-9)

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: 95673-09-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95673-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,7 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95673-09:
(7*9)+(6*5)+(5*6)+(4*7)+(3*3)+(2*0)+(1*9)=169
169 % 10 = 9
So 95673-09-9 is a valid CAS Registry Number.

95673-09-9Upstream product

7769-79-1 2-aminohexadecanoic acid

95673-09-9Downstream Products

95673-09-9Relevant academic research and scientific papers

SYNTHESIS OF (4E,8E,2S,3R,2'R)-N-2'-HYDROXYHEXADECANOYL-9-METHYL-4,8-SPHINGADIENINE, THE CERAMIDE PORTION OF THE FRUITING-INDUCING CEREBROSIDE IN A BASIDIOMYCETE SCHIZOPHYLLUM COMMUNE, AND ITS (2R,3S)-ISOMER

Mori, Kenji,Funaki, Yuji

, p. 2369 - 2378 (2007/10/02)

A synthesis of the natural enantiomer as well as its diastereomer of the title compound was accomplished, confirming the structure proposed for the fruiting-inducing cerebroside of Schizophyllum commune.

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