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2-BROMO-4-(CHLOROMETHYL)THIAZOLE is a heterocyclic, organic chemical compound that is part of the thiazole family. It features a thiazole ring with a bromine atom at the 2nd position and a chloromethyl group at the 4th position. Known for its reactivity and versatility, 2-BROMO-4-(CHLOROMETHYL)THIAZOLE serves as a crucial intermediate in the synthesis of various pharmaceuticals and agrochemicals. Additionally, it finds applications in the production of dyes, pigments, and other chemical products. Due to its potential hazards if mishandled, careful use and handling are essential.

5198-77-6

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5198-77-6 Usage

Uses

Used in Pharmaceutical Industry:
2-BROMO-4-(CHLOROMETHYL)THIAZOLE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-4-(CHLOROMETHYL)THIAZOLE is utilized as an intermediate in the production of agrochemicals. Its properties contribute to the creation of effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.
Used in Dye and Pigment Production:
2-BROMO-4-(CHLOROMETHYL)THIAZOLE is employed as a key component in the manufacturing process of dyes and pigments. Its chemical structure allows for the development of a wide range of colors and hues, making it an essential ingredient in various coloring applications.
Used in Chemical Product Synthesis:
Beyond its applications in pharmaceuticals, agrochemicals, dyes, and pigments, 2-BROMO-4-(CHLOROMETHYL)THIAZOLE is also used in the synthesis of other chemical products. Its versatility and reactivity make it a valuable building block for a diverse array of chemical compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 5198-77-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,9 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5198-77:
(6*5)+(5*1)+(4*9)+(3*8)+(2*7)+(1*7)=116
116 % 10 = 6
So 5198-77-6 is a valid CAS Registry Number.

5198-77-6SDS

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-4-(chloromethyl)-1,3-thiazole

1.2 Other means of identification

Product number -
Other names -

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:5198-77-6 SDS

5198-77-6Downstream Products

5198-77-6Relevant academic research and scientific papers

Hit-to-Lead Optimization of a Novel Class of Potent, Broad-Spectrum Trypanosomacides

Russell, Stephanie,Rahmani, Rapha?l,Jones, Amy J.,Newson, Harriet L.,Neilde, Kevin,Cotillo, Ignacio,Rahmani Khajouei, Marzieh,Ferrins, Lori,Qureishi, Sana,Nguyen, Nghi,Martinez-Martinez, Maria S.,Weaver, Donald F.,Kaiser, Marcel,Riley, Jennifer,Thomas, John,De Rycker, Manu,Read, Kevin D.,Flematti, Gavin R.,Ryan, Eileen,Tanghe, Scott,Rodriguez, Ana,Charman, Susan A.,Kessler, Albane,Avery, Vicky M.,Baell, Jonathan B.,Piggott, Matthew J.

, p. 9686 - 9720 (2016/11/19)

The parasitic trypanosomes Trypanosoma brucei and T. cruzi are responsible for significant human suffering in the form of human African trypanosomiasis (HAT) and Chagas disease. Drugs currently available to treat these neglected diseases leave much to be

Thiepane compounds

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, (2008/06/13)

Tri- and tetra substituted thiepane compositions having use as immunogens, therapeutics, diagnostics and for other industrial purposes are disclosed. The compositions inhibit proteolytic activity of viral enzymes and are useful for the inhibition of such enzymes as well as in assays for the detection of such enzymes. Embodiments in which antigenic polypeptides are bonded to the compositions are useful in raising antibodies against the thiepane haptens or the polypeptide. Labeled thiepanes of this invention are useful as diagnostic reagents.

Thiepane compounds

-

, (2008/06/13)

Tri- and tetra substituted thiepane compositions having use as immunogens, therapeutics, diagnostics and for other industrial purposes are disclosed. The compositions inhibit proteolytic activity of viral enzymes and are useful for the inhibition of such enzymes as well as in assays for the detection of such enzymes. Embodiments in which antigenic polypeptides are bonded to the compositions are useful in raising antibodies against the thiepane haptens or the polypeptide. Labeled thiepanes of this invention are useful as diagnostic reagents.

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