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3-(Chloromethyl)-2,5-dimethylthiophene is an organic compound with the chemical formula C7H9ClS. It is a colorless to pale yellow liquid with a strong, pungent odor. 3-(chloromethyl)-2,5-dimethylthiophene is characterized by the presence of a thiophene ring, which is a five-membered aromatic ring containing one sulfur atom. The molecule has two methyl groups attached to the 2nd and 5th carbon atoms of the thiophene ring, and a chloromethyl group (-CH2Cl) attached to the 3rd carbon atom. This chloromethyl group makes the compound a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is essential to handle 3-(chloromethyl)-2,5-dimethylthiophene with care, as it can undergo various chemical reactions, such as nucleophilic substitution, addition, and elimination reactions.

766-58-5

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766-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 766-58-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 766-58:
(5*7)+(4*6)+(3*6)+(2*5)+(1*8)=95
95 % 10 = 5
So 766-58-5 is a valid CAS Registry Number.

766-58-5SDS

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-Chloromethyl-2,5-dimethyl-thiophene

1.2 Other means of identification

Product number -
Other names -

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

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More Details:766-58-5 SDS

766-58-5Upstream product

766-58-5Relevant academic research and scientific papers

Polyene compounds

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, (2008/06/13)

Novel 9-substituted or unsubstituted thienyl-3,7-dimethyl-nona-2,4,6,8-tetraene derivatives, useful as antitumor agents as well as processes for their preparation and novel intermediates are disclosed.

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