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2-Propenoic acid, 3-cyclohexyl-2-iodo-, methyl ester, (2E)- is a complex organic compound with the chemical formula C10H15IO2. It is a derivative of 2-propenoic acid, featuring a cyclohexyl group at the 3-position and an iodine atom at the 2-position. The molecule is characterized by a double bond (E-configuration) between the 2 and 3 carbon atoms. 2-Propenoic acid, 3-cyclohexyl-2-iodo-, methyl ester, (2E)- is an ester, formed by the reaction of 2-propenoic acid with methanol, where the hydroxyl group of the acid is replaced by a methyl group. It is likely to be used in chemical synthesis or as an intermediate in the production of pharmaceuticals or other specialty chemicals. Due to the presence of the iodine atom, it may also have applications in radiochemistry or as a precursor in the synthesis of other organo-iodine compounds.

126628-75-9

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126628-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126628-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,6,2 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126628-75:
(8*1)+(7*2)+(6*6)+(5*6)+(4*2)+(3*8)+(2*7)+(1*5)=139
139 % 10 = 9
So 126628-75-9 is a valid CAS Registry Number.

126628-75-9SDS

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 methyl 3-cyclohexyl-2-iodoprop-2-enoate

1.2 Other means of identification

Product number -
Other names methyl 3-cyclohexyl-2-iodo-2-propenate

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:126628-75-9 SDS

126628-75-9Relevant academic research and scientific papers

Tetrazolyl-phenyl acetamide glucokinase activators

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, (2008/06/13)

Tetrazolyl-phenyl acetamides are active as glucokinase activators, and are able to increase insulin secretion, which makes them useful for treating type II diabetes.

Tetrazolyl-phenyl acetamide glucokinase activators

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Page column 20, (2010/01/31)

Tetrazolyl-phenyl acetamides are active as glucokinase activators, and are able to increase insulin secretion, which makes them useful for treating type II diabetes.

Trans olefinic glucokinase activators

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Page column 24-25, (2010/02/05)

2,3-Di-substituted trans olefinic N-heteroaromatic or urido propionamides with said substitution at the 2-position being a substituted phenyl group and at the 3-position being a cycloalkyl ring, said propionamides being glucokinase activators which increase insulin secretion in the treatment of type II diabetes.

Heteroaromatic glucokinase activators

-

, (2008/06/13)

2,3-Di-substituted N-heteroaromatic propionamides with said substitution at the 2-position being a substituted phenyl group and at the 3-position being a cycloalkyl ring, said propionamides being glucokinase activators which increase insulin secretion in the treatment of type II diabetes.

An Efficient One Pot Synthesis of α-Iodo-α,β-unsaturated Esters, Ketones and Nitriles via Arsonium Salts

Huang, Yao-Zeng,Shi, Li-Lan,Li, Sao-Wei,Huang, Rong

, p. 2639 - 2646 (2007/10/02)

A number of α-iodo-α,β-unsaturated compounds 3 were synthesized under mild conditions via corresponding readily available arsonium salts 1 in one pot reaction.

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