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Methyl 2-bromo-5-isopropyl-1,3-thiazole-4-carboxylate is a chemical compound characterized by its molecular formula C9H11BrNO2S. It is a synthetic intermediate that plays a crucial role in the production of pharmaceuticals and agrochemicals. Known for its versatile reactivity, Methyl 2-bromo-5-isopropyl-1,3-thiazole-4-carboxylate is extensively utilized in organic synthesis for the preparation of a wide range of heterocyclic compounds. Its significance in the fields of medicinal and agricultural chemistry is underscored by its common use as a building block in the creation of various drugs and pesticides.

81569-28-0

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81569-28-0 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 2-bromo-5-isopropyl-1,3-thiazole-4-carboxylate is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the synthesis of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 2-bromo-5-isopropyl-1,3-thiazole-4-carboxylate serves as a key intermediate in the production of pesticides. Its incorporation into the formulation of these chemicals aids in the development of more effective and targeted pest control solutions, enhancing agricultural productivity and crop protection.
Used in Organic Synthesis:
Methyl 2-bromo-5-isopropyl-1,3-thiazole-4-carboxylate is utilized as a versatile building block in organic synthesis. Its reactivity allows for the preparation of diverse heterocyclic compounds, which are essential in the creation of complex organic molecules with various applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 81569-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,6 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81569-28:
(7*8)+(6*1)+(5*5)+(4*6)+(3*9)+(2*2)+(1*8)=150
150 % 10 = 0
So 81569-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H10BrNO2S/c1-4(2)6-5(7(11)12-3)10-8(9)13-6/h4H,1-3H3

81569-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-bromo-5-isopropylthiazole-4-carboxylate

1.2 Other means of identification

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

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:81569-28-0 SDS

81569-28-0Downstream Products

81569-28-0Relevant academic research and scientific papers

IMIDAZOTHIADIAZOLE AND IMIDAZOPYRAZINE DERIVATIVES AS PROTEASE ACTIVATED RECEPTOR 4 (PAR4) INHIBITORS FOR TREATING PLATELET AGGREGATION

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Paragraph 00192, (2013/11/18)

The present invention provides thiazole compounds of Formula I wherein W, Y, R0, R2, R4, R5, R6, R7, X1, X2, X3 and X4 are as defined herein, or a stereoisomer, tautomer, pharmaceutically acceptable salt, prodrug ester or solvate form thereof, wherein all of the variables are as defined herein. These compounds are inhibitors of platelet aggregation and thus can be used as medicaments for treating or preventing thromboembolic disorders.

The Preparation of Thiazole-4- and -5-carboxylates, and an Infrared Study of their Rotational Isomers

Barton, Anne,Breukelman, Stephen P.,Kaye, Perry T.,Meakins, G. Denis,Morgan, David J.

, p. 159 - 164 (2007/10/02)

Convenient general procedures have been developed for preparing series of thiazole-4- and -5-carboxylates containing alkyl and halogeno substituents.While both series of esters show i.r. carbonyl doublets caused by rotational isomerism, the more intense absorptions of the 4-carboxylates are the lower wavenumber components, whereas those of the 5-carboxylates are the higher wavenumber components.In both series the stronger bands arise from the thermochemically more stable forms; identification of these forms as the carbonyl O,S-syn-s-trans rotamers is more certain with the 4-carboxylates than with the 5-carboxylates.

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