Cas 176384-40-0,(Z)-2-Acetylamino-4-benzyloxy-but-2-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

176384-40-0

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Basic information

Product Name: (Z)-2-Acetylamino-4-benzyloxy-but-2-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
Synonyms: (Z)-2-Acetylamino-4-benzyloxy-but-2-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
CAS NO:176384-40-0
Molecular Formula:
Molecular Weight: 463.617
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: (Z)-2-Acetylamino-4-benzyloxy-but-2-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-Acetylamino-4-benzyloxy-but-2-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(176384-40-0)
EPA Substance Registry System: (Z)-2-Acetylamino-4-benzyloxy-but-2-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(176384-40-0)

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: 176384-40-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 176384-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,3,8 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 176384-40:
(8*1)+(7*7)+(6*6)+(5*3)+(4*8)+(3*4)+(2*4)+(1*0)=160
160 % 10 = 0
So 176384-40-0 is a valid CAS Registry Number.

176384-40-0Upstream product

65253-04-5 (-)-8-phenylmenthol

176384-40-0Downstream Products

176384-42-2 (2R,3S)-2-Acetylamino-4-benzyloxy-3-phenylsulfanyl-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

176384-40-0Relevant academic research and scientific papers

Diastereoselective synthesis of triacetyl-L-erythro-C18-sphingosine

Miyata,Yamaguchi,Ninomiya,Naito,Okamura

, p. 636 - 638 (1996)

A new stereoselective synthetic route to triacetyl-L-erythro-C18- sphingosine has been developed by the combination of diastereoselective addition of thiophenol to chiral olefins and subsequent intramolecular substitution of the corresponding sulfonium group.

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