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2-Cyclopropene-1-carboxylic acid, 2,3-diethyl-methyl ester is a complex organic compound with the chemical formula C9H14O2. It is a derivative of cyclopropene-1-carboxylic acid, featuring a cyclopropane ring fused to a cyclopentane ring, with two ethyl groups attached at the 2 and 3 positions, and a methyl ester group at the 1 position. 2-Cyclopropene-1-carboxylic acid, 2,3-diethyl-, methyl ester is characterized by its unique molecular structure, which contributes to its distinct chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. Due to its specific functional groups and structural features, it may exhibit unique reactivity and stability, making it a subject of interest for researchers in organic chemistry.

7382-02-7

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7382-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7382-02-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7382-02:
(6*7)+(5*3)+(4*8)+(3*2)+(2*0)+(1*2)=97
97 % 10 = 7
So 7382-02-7 is a valid CAS Registry Number.

7382-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl-2,3 cyclopropene-2 carboxylate de methyle

1.2 Other means of identification

Product number -
Other names methyl 2,3-diethyl-2-cyclopropene-1-carboxylate

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 -
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More Details:7382-02-7 SDS

7382-02-7Relevant academic research and scientific papers

Ethers allyliques. Reactivite des ethers α-cyclopropeniques en milieu basique

Vincens, Maurice,Vidal, Michel

, p. 900 - 904 (2007/10/02)

In basic, protic medium, the exocyclic migration of the double bond in esters of 2-methoxymethyl 3-alkyl 2-cyclopropenecarboxylic acids is highly regioselective, yielding only 2-methoxymethyl 3-alkylidene cyclopropanecarboxylic acids.The reaction is, in addition, stereospecific, leading to the trans isomer as the sole product.The exocyclic migration of the double bond appears to be irreversible and therefore the formation of enol ethers is not observed.

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