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16488-62-3

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16488-62-3 Usage

General Description

2,3,5-triiodo-4-methyl-Thiophene is a chemical compound that contains three iodine atoms, a methyl group, and a thiophene ring. Thiophene is a heterocyclic compound that consists of a five-membered ring with four carbon atoms and one sulfur atom. The addition of three iodine atoms and a methyl group to the thiophene ring enhances its reactivity and introduces new chemical properties. 2,3,5-triiodo-4-methyl-Thiophene is commonly used in the synthesis of organic molecules and pharmaceuticals due to its unique structure and reactivity. Additionally, it can also be used as a precursor in the production of various materials and chemicals.

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 articles and documents

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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