Cas 178232-05-8,(Z)-(R)-6-Benzyloxy-2-[((S)-2-methoxy-propionyl)-((S)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester

178232-05-8

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Basic information

Product Name: (Z)-(R)-6-Benzyloxy-2-[((S)-2-methoxy-propionyl)-((S)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester
Synonyms:
CAS NO:178232-05-8
Molecular Formula:
Molecular Weight: 439.552
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)-(R)-6-Benzyloxy-2-[((S)-2-methoxy-propionyl)-((S)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-(R)-6-Benzyloxy-2-[((S)-2-methoxy-propionyl)-((S)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester(178232-05-8)
EPA Substance Registry System: (Z)-(R)-6-Benzyloxy-2-[((S)-2-methoxy-propionyl)-((S)-1-phenyl-ethyl)-amino]-hex-4-enoic acid methyl ester(178232-05-8)

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: 178232-05-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 178232-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,2,3 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 178232-05:
(8*1)+(7*7)+(6*8)+(5*2)+(4*3)+(3*2)+(2*0)+(1*5)=138
138 % 10 = 8
So 178232-05-8 is a valid CAS Registry Number.

178232-05-8Upstream product

178232-05-8Downstream Products

159247-18-4 (+)-bulgecinine

178232-05-8Relevant academic research and scientific papers

An improved procedure for the enantioselective synthesis of (+)- and (-)-cis-4-hydroxyprolines and bulgecinines

Graziani, Lucia,Porzi, Gianni,Sandri, Sergio

, p. 1341 - 1346 (1996)

An efficient enantioselective synthesis of both the enantiomers of cis-4-hydroxy-proline and bulgecinine was accomplished starting from synthons 1 or 1'. The improved synthetic route to the aforesaid enantiomerically pure proline derivatives was established via a stereocontrolled double iodocyclization of 3(a,b) or 3'(a,b).

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