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1,1-Cyclopropanedicarboxylic acid, 2-(1-methylethenyl)-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61111-65-7

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61111-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61111-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,1 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61111-65:
(7*6)+(6*1)+(5*1)+(4*1)+(3*1)+(2*6)+(1*5)=77
77 % 10 = 7
So 61111-65-7 is a valid CAS Registry Number.

61111-65-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-prop-1-en-2-ylcyclopropane-1,1-dicarboxylate

1.2 Other means of identification

Product number -
Other names dimethyl 2-isopropenyl-1,1-cyclopropanedicarboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61111-65-7 SDS

61111-65-7Relevant academic research and scientific papers

ALKYLATION OF CH ACIDS IN THE PRESENCE OF POTASSIUM CARBONATE. III. ALKYLATION OF CH ACIDS BY 2,3-SUBSTITUTED 1,4-DIBROMO-2-BUTENES

Vardapetyan, A. A.,Khachatryan, D. S.,Morlyan, N. M.

, p. 1237 - 1242 (2007/10/02)

During the cycloalkylation of CH acids by 2,3-substituted (methyl-chlorine) 1,4-dibromo-2-butenes the direction of intramolecular C- and O-alkylation depends both on steric and on electronic factors.The introduction of substituents into the alkylating agent and the presence of acetyl groups in the initial CH acids promote regiospecific intramolecular O-alkylation.

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