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Dimethyl cyclohex-3-ene-1,6-dicarboxylate is a chemical compound with the molecular formula C10H14O4. It is a diester derived from cyclohexene, featuring a six-membered carbon ring with a double bond between the third and fourth carbon atoms. The molecule has two carboxylate groups (-COO-) attached to the first and sixth carbon atoms, with two methyl groups (-CH3) esterifying these carboxylate groups. This organic compound is known for its versatile applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is typically synthesized through the reaction of cyclohexane-1,6-dicarboxylic acid with methanol in the presence of a catalyst. Dimethyl cyclohex-3-ene-1,6-dicarboxylate is an important intermediate in the production of certain polymers and can also be used as a building block in the creation of complex organic molecules.

7500-55-2

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7500-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7500-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7500-55:
(6*7)+(5*5)+(4*0)+(3*0)+(2*5)+(1*5)=82
82 % 10 = 2
So 7500-55-2 is a valid CAS Registry Number.

7500-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl 4-cyclohexene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 4-Cyclohexene-1,2-dicarboxylic acid dimethyl ester

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:7500-55-2 SDS

7500-55-2Relevant academic research and scientific papers

Compelling P1 substituent affect on metalloprotease binding profile enables the design of a novel cyclohexyl core scaffold with excellent MMP selectivity and HER-2 sheddase inhibition

Burns, David M.,Li, Yun-Long,Shi, Eric,He, Chunhong,Xu, Meizhong,Zhuo, Jincong,Zhang, Colin,Qian, Ding-Quan,Li, Yanlong,Wynn, Richard,Covington, Maryanne B.,Katiyar, Kamna,Marando, Cindy A.,Fridman, Jordan S.,Scherle, Peggy,Friedman, Steve,Metcalf, Brian,Yao, Wenqing

scheme or table, p. 3525 - 3530 (2010/03/24)

A serendipitous discovery that the metalloprotease binding profile of a novel class of 2-carboxamide-3-hydroxamic acid piperidines could be significantly attenuated by the modification of the unexplored P1 substituent enabled the design and synthesis of a

Construction of bicyclo[2.2.2]octane ring system via homoallyl-homoallyl radical rearrangement

Toyota, Masahiro,Yokota, Masahiro,Ihara, Masataka

, p. 1551 - 1554 (2007/10/03)

We designed a sequential three-step, one-pot reaction (homoallyl- homoallyl radical rearrangement reaction) to generate highly functionalized bicyclo[2.2.2]octane ring system, and succeeded in developing a novel synthetic method to bicyclo[2.2.2]octane compounds from simple cyclohexene derivatives.

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