Cas 165067-79-8,Cyclopentanone, 2-acetyl-4-(1-methylethenyl)-, (2S-trans)- (9CI)

165067-79-8

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Basic information

Product Name: Cyclopentanone, 2-acetyl-4-(1-methylethenyl)-, (2S-trans)- (9CI)
Synonyms: Cyclopentanone, 2-acetyl-4-(1-methylethenyl)-, (2S-trans)- (9CI)
CAS NO:165067-79-8
Molecular Formula: C10H14O2
Molecular Weight: 166.21696
EINECS: N/A
Product Categories: ACETYLGROUP
Mol File: 165067-79-8.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Cyclopentanone, 2-acetyl-4-(1-methylethenyl)-, (2S-trans)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Cyclopentanone, 2-acetyl-4-(1-methylethenyl)-, (2S-trans)- (9CI)(165067-79-8)
EPA Substance Registry System: Cyclopentanone, 2-acetyl-4-(1-methylethenyl)-, (2S-trans)- (9CI)(165067-79-8)

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: 165067-79-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 165067-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,0,6 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 165067-79:
(8*1)+(7*6)+(6*5)+(5*0)+(4*6)+(3*7)+(2*7)+(1*9)=148
148 % 10 = 8
So 165067-79-8 is a valid CAS Registry Number.

165067-79-8Upstream product

165173-38-6 1-((R)-2-Amino-4-isopropenyl-cyclopent-1-enyl)-ethanone

165067-79-8Downstream Products

165067-79-8Relevant academic research and scientific papers

New Chiral Agents for Resolution of Racemic cis-Permethric and cis-Z-cyhalothric Acids

Popov, Sergey A.,Tkachev, Alexey V.

, p. 1013 - 1018 (1995)

Resolution of racemic pyrethroid acids (cis-permethric and cis-Z-cyhalothric) using stable optically active amines derived from natural monoterpene (+)-3-carene and preparation of optically active esters of the pyrethroid acids are described.

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