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19259-10-0

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19259-10-0 Usage

General Description

2,3,5-Triiodothiophene is a chemical compound with the molecular formula C4H2I3S. It is a member of the thiophene family, which consists of a five-membered ring containing four carbon atoms and one sulfur atom. The presence of three iodine atoms on the thiophene ring gives 2,3,5-Triiodothiophene unique properties and makes it useful in various chemical and pharmaceutical applications. 2,3,5-Triiodothiophene is often used as a building block in the synthesis of organic compounds, particularly in the development of new materials and pharmaceuticals. Its iodine atoms make it highly reactive, allowing it to participate in a wide range of chemical reactions. 2,3,5-Triiodothiophene is of interest in the field of organic chemistry due to its potential for creating novel, functional materials and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 19259-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19259-10:
(7*1)+(6*9)+(5*2)+(4*5)+(3*9)+(2*1)+(1*0)=120
120 % 10 = 0
So 19259-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C4HI3S/c5-2-1-3(6)8-4(2)7/h1H

19259-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-Triiodothiophene

1.2 Other means of identification

Product number -
Other names 2,3,5-Trijodthiophen

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:19259-10-0 SDS

19259-10-0Relevant articles and documents

Selective metallation of 3-halothiophenes: Practical methods for the synthesis of 2-bromo-3-formylthiophene

Sonoda, Motohiro,Kinoshita, Shoko,Luu, Thanh,Fukuda, Hiroshi,Miki, Koji,Umeda, Rui,Tobe, Yoshito

experimental part, p. 3315 - 3323 (2011/03/20)

Selective lithiation of 3-bromothiophene was accomplished under controlled conditions without formation of undesired thienyllithium compounds. A thienyl Grignard reagent derived from 2-bromo-3-iodothiophene was transformed into 2-bromo-3-formylthiophene in high selectivity by formylation with dimethylformamide (DMF) at optimal reaction temperature. Copyright Taylor & Francis Group, LLC.

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