Cas 187875-77-0,(5S)-4-(benzyloxycarbonyl)-2-isopropylidene-5-phenyl-3-cyclopentanone

187875-77-0

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Basic information

Product Name: (5S)-4-(benzyloxycarbonyl)-2-isopropylidene-5-phenyl-3-cyclopentanone
Synonyms: (5S)-4-(benzyloxycarbonyl)-2-isopropylidene-5-phenyl-3-cyclopentanone
CAS NO:187875-77-0
Molecular Formula:
Molecular Weight: 332.399
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: (5S)-4-(benzyloxycarbonyl)-2-isopropylidene-5-phenyl-3-cyclopentanone(CAS DataBase Reference)
NIST Chemistry Reference: (5S)-4-(benzyloxycarbonyl)-2-isopropylidene-5-phenyl-3-cyclopentanone(187875-77-0)
EPA Substance Registry System: (5S)-4-(benzyloxycarbonyl)-2-isopropylidene-5-phenyl-3-cyclopentanone(187875-77-0)

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: 187875-77-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 187875-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,8,7 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 187875-77:
(8*1)+(7*8)+(6*7)+(5*8)+(4*7)+(3*5)+(2*7)+(1*7)=210
210 % 10 = 0
So 187875-77-0 is a valid CAS Registry Number.

187875-77-0Upstream product

201230-82-2 carbon monoxide

187875-77-0Downstream Products

187875-77-0Relevant academic research and scientific papers

Catalytic asymmetric [4 + 1] cycloaddition of vinylallenes with carbon monoxide: Reversal of the induced chirality by the choice of metal

Murakami, Masahiro,Itami, Kenichiro,Ito, Yoshihiko

, p. 4130 - 4135 (2007/10/03)

Rhodium(I) and platinum(0) complexes having a chiral ligand, 1,2-bis(2,5-dialkylphosphorano)-benzene, effected an asymmetric carbonylative [4 + 1] cycloaddition reaction of vinylallenes. Useful levels of asymmetric induction were attained even with substr

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