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2,3,5-triiodo-4-methyl-Thiophene is a chemical compound that features a thiophene ring with three iodine atoms and a methyl group attached to it. Thiophene is a heterocyclic compound composed of a five-membered ring with four carbon atoms and one sulfur atom. The presence of the iodine atoms and the methyl group significantly enhances the reactivity and chemical properties of the molecule.

16488-62-3

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16488-62-3 Usage

Uses

Used in Pharmaceutical Synthesis:
2,3,5-triiodo-4-methyl-Thiophene is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs with specific therapeutic properties.
Used in Organic Chemistry:
In the field of organic chemistry, 2,3,5-triiodo-4-methyl-Thiophene serves as a versatile building block for the creation of complex organic molecules. Its ability to participate in various chemical reactions allows for the synthesis of a wide range of organic compounds.
Used as a Precursor in Material Production:
2,3,5-triiodo-4-methyl-Thiophene also functions as a precursor in the production of different materials and chemicals. Its unique chemical properties enable it to be transformed into a variety of useful substances, contributing to the advancement of various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 16488-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,8 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16488-62:
(7*1)+(6*6)+(5*4)+(4*8)+(3*8)+(2*6)+(1*2)=133
133 % 10 = 3
So 16488-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H3I3S/c1-2-3(6)5(8)9-4(2)7/h1H3

16488-62-3SDS

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 2,3,5-triiodo-4-methylthiophene

1.2 Other means of identification

Product number -
Other names 2,3,5-triiodo-4-methyl-thiophene

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:16488-62-3 SDS

16488-62-3Upstream product

16488-62-3Downstream Products

16488-62-3Relevant academic research and scientific papers

Halogenation Using Quaternary Ammonium Polyhalides. XXXI. Halogenation of Thiophene Derivatives with Benzyltrimethylammonium Polyhalides

Okamoto, Tsuyoshi,Kakinami, Takaaki,Fujimoto, Hiroshi,Kajigaeshi, Shoji

, p. 2566 - 2568 (2007/10/02)

The reactions of thiophene derivatives with benzyltrimethylammonium tetrachloroiodate, benzyltrimethylammonium tribromide, and benzyltrimethylammonium dichloroiodate in acetic acid or in acetic acid-zinc chloride under mild conditions gave chloro-, bromo-, and iodo-substituted thiophene derivatives, respectively, in satifactory yields.

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