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Thiazole, 5-bromo-4-(1-methylethyl)-, also known as 5-bromo-4-isopropylthiazole, is a chemical compound belonging to the thiazole class of heterocyclic compounds. It features a five-membered ring structure with the formula C3H3NS, incorporating a nitrogen atom and a sulfur atom. This specific derivative is characterized by the presence of a bromine atom at the 5th position and an isopropyl group at the 4th position. The unique structural features and potential reactivity of the bromine atom make Thiazole, 5-broMo-4-(1-Methylethyl)- a versatile molecule with a wide range of applications in various industries.

1025700-46-2

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1025700-46-2 Usage

Uses

Used in Pharmaceutical Industry:
Thiazole, 5-bromo-4-(1-methylethyl)-, is used as a pharmaceutical intermediate for the synthesis of various therapeutic agents. Its unique structure and potential pharmacological properties make it a valuable building block in the development of new drugs with diverse therapeutic applications, such as antimicrobial, anti-inflammatory, and anticancer agents.
Used in Agrochemical Industry:
In the agrochemical industry, this specific thiazole derivative is employed as a key intermediate in the synthesis of agrochemicals, including pesticides and herbicides. Its chemical reactivity and structural features contribute to the development of effective and targeted agrochemicals for crop protection and management.
Used in Dyes and Pigments Industry:
Thiazole, 5-bromo-4-(1-methylethyl)-, is utilized as a key component in the formulation of dyes and pigments due to its unique color properties and stability. Its incorporation into dye and pigment formulations enhances their performance, making them suitable for various applications, such as textiles, plastics, and printing inks.
Used in Research and Development:
This thiazole derivative is also used in research and development settings for the exploration of its chemical properties, reactivity, and potential applications in various fields. Its unique structure and bromine atom provide opportunities for studying its interactions with other molecules and its potential use in the synthesis of novel compounds with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1025700-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,7,0 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1025700-46:
(9*1)+(8*0)+(7*2)+(6*5)+(5*7)+(4*0)+(3*0)+(2*4)+(1*6)=102
102 % 10 = 2
So 1025700-46-2 is a valid CAS Registry Number.

1025700-46-2SDS

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 5-Bromo-4-isopropylthiazole

1.2 Other means of identification

Product number -
Other names 5-bromo-4-propan-2-yl-1,3-thiazole

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:1025700-46-2 SDS

1025700-46-2Relevant academic research and scientific papers

THIAZOLE AND OXAZOLE-SUBSTITUTED ARYLAMIDES AS P2X3 AND P2X2/3 ANTAGONISTS

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, (2012/02/03)

Compounds of the formula I: or a pharmaceutically acceptable salt thereof, wherein, R1 is a group of formula A or formula B, and X, R2, R3, R4, R5, R6, Ra and Rb are as defined herein. Also provided are methods of using the compounds for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist and methods of making the subject compounds.

THIAZOLE AND OXAZOLE-SUBSTITUTED ARYLAMIDES

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Page/Page column 62; 63, (2008/12/05)

Compounds of the formula (I) or a pharmaceutically acceptable salt thereof, wherein: R1 is a group of formula A or formula B; and X, R2, R3, R4, R5, R6, Ra and Rb are as defined herein. Also provided are methods of using the compounds for treating diseases mediated by a P2X3 and/or a P2X2/3 receptor antagonist and methods of making the subject compounds.

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