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2-BROMO-4-CYANOTHIAZOLE is a brominated derivative of 4-cyanothiazole, a chemical compound with the molecular formula C5H3BrN2S. It is a white to off-white crystalline solid, characterized by a molecular weight of 200.06 g/mol and a melting point of approximately 120-124°C. 2-BROMO-4-CYANOTHIAZOLE is widely recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and also serves as a building block in the production of dyes, pigments, and other organic compounds.

848501-90-6

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848501-90-6 Usage

Uses

Used in Pharmaceutical Industry:
2-BROMO-4-CYANOTHIAZOLE is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of a diverse range of medicinal compounds with potential applications in treating various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-4-CYANOTHIAZOLE is utilized as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these products aids in enhancing their effectiveness in protecting crops and managing pests, thereby contributing to increased agricultural productivity.
Used in Dye and Pigment Production:
2-BROMO-4-CYANOTHIAZOLE serves as a building block in the manufacturing process of dyes and pigments, which are essential for a variety of applications across different industries. Its chemical properties enable the creation of vibrant and stable colorants used in textiles, plastics, inks, and other materials.
Used in Organic Compound Synthesis:
Beyond its applications in pharmaceuticals, agrochemicals, dyes, and pigments, 2-BROMO-4-CYANOTHIAZOLE is also employed as a versatile intermediate in the synthesis of other organic compounds. Its reactivity and structural features make it a valuable component in the development of novel chemical entities with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 848501-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,5,0 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 848501-90:
(8*8)+(7*4)+(6*8)+(5*5)+(4*0)+(3*1)+(2*9)+(1*0)=186
186 % 10 = 6
So 848501-90-6 is a valid CAS Registry Number.
InChI:InChI=1/C4HBrN2S/c5-4-7-3(1-6)2-8-4/h2H

848501-90-6SDS

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-bromo-1,3-thiazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-bromothiazole-4-carbonitrile

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:848501-90-6 SDS

848501-90-6Downstream Products

848501-90-6Relevant articles and documents

Corresponding amine nitrile and method of manufacturing thereof

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Paragraph 0150; 0151; 0152; 0162, (2018/05/07)

The invention relates to a manufacturing method of nitrile. Compared with the prior art, the manufacturing method has the characteristics of significantly reduced using amount of an ammonia source, low environmental pressure, low energy consumption, low production cost, high purity and yield of a nitrile product and the like, and nitrile with a more complex structure can be obtained. The invention also relates to a method for manufacturing corresponding amine from nitrile.

NUCLEAR TRANSPORT MODULATIORS AND USES THEREOF

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Page/Page column 225, (2011/10/03)

The invention generally relates to the field of nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to new substituted-heterocyclic azole compounds, the synthesis and use of these compounds and their pharmaceutical compositions, e.g

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