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5-Bromo-2-iodothiazole is a heterocyclic chemical compound with the molecular formula C4H2BrINS. It features the presence of both bromine and iodine halogens, which contribute to its unique properties and potential applications across various fields.

108306-64-5

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108306-64-5 Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
5-Bromo-2-iodothiazole is utilized as a building block in the synthesis of pharmaceuticals and agrochemicals. Its unique structure allows for the creation of new drugs with potential therapeutic and pesticidal properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-Bromo-2-iodothiazole serves as a starting material for the development of novel drugs. Its chemical properties and reactivity make it a valuable component in the design and synthesis of innovative pharmaceutical compounds.
Used in Materials Science for Electronic and Optoelectronic Devices:
5-Bromo-2-iodothiazole is also employed in materials science, particularly in the development of new materials for electronic and optoelectronic devices. Its halogens and heterocyclic structure contribute to the compound's electronic and optical properties, making it suitable for use in advanced device technologies.
Research and Development:
Due to its unique structure and potential for various applications, 5-Bromo-2-iodothiazole has garnered significant attention in research and development. Scientists and researchers are exploring its properties and potential uses in diverse industries, further expanding its applications and significance in the scientific community.

Check Digit Verification of cas no

The CAS Registry Mumber 108306-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,0 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108306-64:
(8*1)+(7*0)+(6*8)+(5*3)+(4*0)+(3*6)+(2*6)+(1*4)=105
105 % 10 = 5
So 108306-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C3HBrINS/c4-2-1-6-3(5)7-2/h1H

108306-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-2-iodo-1,3-thiazole

1.2 Other means of identification

Product number -
Other names Thiazole,5-bromo-2-iodo

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:108306-64-5 SDS

108306-64-5Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLE COMPOUNDS AS TOLL RECEPTOR INHIBITORS

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Page/Page column 354-355, (2021/05/07)

Disclosed are compounds of Formula (I) N-oxides, or salts thereof, wherein G, A, R1, and R5 are defined herein. Also disclosed are methods of using such compounds as inhibitors of signaling through Toll-like receptor 7, or 8, or 9, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating inflammatory and autoimmune diseases.

1-(HET)ARYLSULFONYL-(PYRROLIDINE OR PIPERIDINE)-2-CARBOXAMIDE DERIVATIVES AND THEIR USE AS TRPA1 ANTAGONISTS

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Paragraph 0850; 0851; 0852, (2016/09/22)

The invention is concerned with the compounds of formula I and salts thereof and other compounds of formulas II-IX as disclosed herein. In addition, the present invention relates to methods of manufacturing and methods of using the compounds of formulas I-IX as well as pharmaceutical compositions containing such compounds. The compounds may be useful in treating diseases and conditions mediated by TRPA1, such as pain or asthma.

Synthesis of Stannylthiazoles and Mixed Stannylsilylthiazoles and their Use for a Convenient Preparation of Mono- and Bis-halothiazoles

Dondoni, A.,Mastellari, A. R.,Medici, A.,Negrini, E.,Pedrini, P.

, p. 757 - 760 (2007/10/02)

Stannylthiazoles and stannyl-silylthiazoles have been prepared and employed as thiazolyl carbanion equivalents in reactions with halogens to give mono- and mixed bis-halothiazoles in good yields.

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