Cas 149228-51-3,(E)-(3R,6R)-6-Benzyl-7-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-cyclohexylmethyl-7-oxo-hept-4-enoic acid ethyl ester

149228-51-3

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Basic information

Product Name: (E)-(3R,6R)-6-Benzyl-7-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-cyclohexylmethyl-7-oxo-hept-4-enoic acid ethyl ester
Synonyms: (E)-(3R,6R)-6-Benzyl-7-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-cyclohexylmethyl-7-oxo-hept-4-enoic acid ethyl ester
CAS NO:149228-51-3
Molecular Formula:
Molecular Weight: 531.692
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: (E)-(3R,6R)-6-Benzyl-7-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-cyclohexylmethyl-7-oxo-hept-4-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(3R,6R)-6-Benzyl-7-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-cyclohexylmethyl-7-oxo-hept-4-enoic acid ethyl ester(149228-51-3)
EPA Substance Registry System: (E)-(3R,6R)-6-Benzyl-7-((R)-4-benzyl-2-oxo-oxazolidin-3-yl)-3-cyclohexylmethyl-7-oxo-hept-4-enoic acid ethyl ester(149228-51-3)

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: 149228-51-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 149228-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,2,2 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 149228-51:
(8*1)+(7*4)+(6*9)+(5*2)+(4*2)+(3*8)+(2*5)+(1*1)=143
143 % 10 = 3
So 149228-51-3 is a valid CAS Registry Number.

149228-51-3Upstream product

149228-51-3Downstream Products

149228-58-0 (E)-(2R,5R)-2-Benzyl-5-cyclohexylmethyl-hept-3-enedioic acid 7-ethyl ester

149228-51-3Relevant academic research and scientific papers

A concise and enantioselective synthesis of novel HIV-1 protease transition state mimics

Dorsey,Plzak,Ball

, p. 1851 - 1854 (1993)

Novel HIV-1 protease inhibitors have been prepared in an enantioselective manner via an Evans asymmetric aldol, Claisen rearrangement and iodolactonization. X-ray crystallographic analysis was used to confirm the absolute configuration of the newly created stereogenic centers.

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