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Dimethyl (2Z)-2-iodobut-2-enedioate is a chemical compound with the molecular formula C6H7IO4. It is an organic iodine-containing compound that features a butenedioic acid backbone with a double bond in the 2Z configuration, indicating the presence of a cis-geometry around the double bond. The molecule also includes two methyl ester groups attached to the carboxylic acid groups, which contribute to its overall structure. dimethyl (2Z)-2-iodobut-2-enedioate is known for its potential applications in various chemical reactions and synthetic processes, particularly in the field of organic synthesis. It is important to note that due to the presence of iodine, dimethyl (2Z)-2-iodobut-2-enedioate may have unique reactivity and properties that can be exploited in specific chemical transformations.

1600-35-7

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1600-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1600-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1600-35:
(6*1)+(5*6)+(4*0)+(3*0)+(2*3)+(1*5)=47
47 % 10 = 7
So 1600-35-7 is a valid CAS Registry Number.

1600-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl (Z)-2-iodobut-2-enedioate

1.2 Other means of identification

Product number -
Other names Jodfumarsaeure-dimethylester

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:1600-35-7 SDS

1600-35-7Downstream Products

1600-35-7Relevant academic research and scientific papers

Stereoselective hydrohalogenation of alkynoic acids and their esters in ionic liquids

Salazar, Jose,Fernandez, Francys,Restrepo, Jelem,Lopez, Simon E.

, p. 170 - 172 (2008/02/12)

A novel procedure is described for the hydrohalogenation of alkynoic acids and their esters using N-alkylpyridinium ionic liquids. Hydrohalogenating agents were prepared by mixing N-alkylpyridinium halides with an equimolar amount of trifluoroacetic acid.

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