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3-Cyclopentene-1-carboxylic acid, 3-methyl-, ethyl ester (8CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15215-84-6

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15215-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15215-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,1 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15215-84:
(7*1)+(6*5)+(5*2)+(4*1)+(3*5)+(2*8)+(1*4)=86
86 % 10 = 6
So 15215-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O2/c1-3-11-9(10)8-5-4-7(2)6-8/h4,8H,3,5-6H2,1-2H3

15215-84-6SDS

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 3-Methyl-3-cyclopenten-1-carbonsaeure-ethylester

1.2 Other means of identification

Product number -
Other names 3-Cyclopentene-1-carboxylic acid,3-methyl-,ethyl ester (8CI,9CI)

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:15215-84-6 SDS

15215-84-6Relevant academic research and scientific papers

Kinetic benchmarking reveals the competence of prenyl groups in ring-closing metathesis

Bahou, Karim A.,Braddock, D. Christopher,Meye, Adam G.,Savage, G. Paul

, p. 5332 - 5335 (2017)

A series of prenyl-containing malonates are kinetically benchmarked against the standard allyl-containing congeners using a ruthenium benzylidene precatalyst for ringclosing metatheses. The prenyl grouping is found to be a superior acceptor olefin compared to an allyl group in RCM processes with ruthenium alkylidenes derived from terminal alkenes. The prenyl group is also found to be a highly competent acceptor for a ruthenium alkylidene derived from a 1, 1-disubstituted olefin in a RCM process.

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