Cas 96358-59-7,Cyclopropanecarboxylic acid, 2-ethenyl-2-methyl-, methyl ester, cis- (9CI)

96358-59-7

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Basic information

Product Name: Cyclopropanecarboxylic acid, 2-ethenyl-2-methyl-, methyl ester, cis- (9CI)
Synonyms: Cyclopropanecarboxylic acid, 2-ethenyl-2-methyl-, methyl ester, cis- (9CI)
CAS NO:96358-59-7
Molecular Formula: C8H12O2
Molecular Weight: 140.17968
EINECS: N/A
Product Categories: CARBOXYLICESTER
Mol File: 96358-59-7.mol
Article Data: 2

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: Cyclopropanecarboxylic acid, 2-ethenyl-2-methyl-, methyl ester, cis- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Cyclopropanecarboxylic acid, 2-ethenyl-2-methyl-, methyl ester, cis- (9CI)(96358-59-7)
EPA Substance Registry System: Cyclopropanecarboxylic acid, 2-ethenyl-2-methyl-, methyl ester, cis- (9CI)(96358-59-7)

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: 96358-59-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96358-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,5 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96358-59:
(7*9)+(6*6)+(5*3)+(4*5)+(3*8)+(2*5)+(1*9)=177
177 % 10 = 7
So 96358-59-7 is a valid CAS Registry Number.

96358-59-7Upstream product

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96358-59-7Relevant articles and documents

New catalytic system Cu(OAc)2-2,4-lutidine-ZnCl2 for olefin cyclopropanation with methyl diazoacetate

Gareev,Sultanova,Biglova,Dokichev,Tomilov

experimental part, p. 1784 - 1786 (2011/04/23)

A new efficient catalytic system consisting of Cu(OAc)2, 2,4-lutidine, and ZnCl2 was found for the cyclopropanation of unsaturated compounds with methyl diazoacetate. In the case of conjugated dienes, the process occurs regioselectively at the most alkylated C=C bond.

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