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2-Bromo-5-cyclopropylthiazole, a chemical compound with the molecular formula C6H6BrNS, is a thiazole derivative that features a bromine atom and a cyclopropyl group. 2-broMo-5-cyclopropylthiazole is recognized for its potential applications in various fields due to its unique structural properties.

1086381-69-2

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1086381-69-2 Usage

Uses

Used in Pharmaceutical and Chemical Research:
2-Bromo-5-cyclopropylthiazole is utilized as a building block in the synthesis of various biologically active compounds, contributing to the development of new pharmaceutical agents.
Used in Antimicrobial and Anti-Fungal Applications:
Leveraging its inherent properties, 2-bromo-5-cyclopropylthiazole is applied as an antimicrobial and anti-fungal agent, serving to combat microbial infections and fungal growth.
Used in Agriculture:
In the agricultural industry, 2-bromo-5-cyclopropylthiazole is used as a pesticide and herbicide, capitalizing on its ability to inhibit the growth of certain plant pathogens, thereby protecting crops from diseases and unwanted plant growth.
Used in Chemical Industry:
2-broMo-5-cyclopropylthiazole also finds use in the chemical industry for various purposes, including the creation of intermediates for chemical synthesis, taking advantage of its reactive bromine atom and cyclopropyl group.

Check Digit Verification of cas no

The CAS Registry Mumber 1086381-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,3,8 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1086381-69:
(9*1)+(8*0)+(7*8)+(6*6)+(5*3)+(4*8)+(3*1)+(2*6)+(1*9)=172
172 % 10 = 2
So 1086381-69-2 is a valid CAS Registry Number.

1086381-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromo-2-cyclopropyl-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 4-bromo-2-cyclopropylthiazole

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:1086381-69-2 SDS

1086381-69-2Relevant academic research and scientific papers

HETEROCYCLIC COMPOUND AND ARTHROPOD PEST CONTROL COMPOSITION CONTAINING SAME

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Paragraph 0631-0632; 0639-0640, (2021/02/05)

The present invention provides a compound that has an excellent control effect on arthropod pests, and is represented by formula (I) [wherein Q represents a group represented by Q1, or the like, n is 0, 1, or 2, R2 represents a C1-C6 alkyl grou

BENZIMIDAZOLE COMPOUNDS AND USE THEREOF FOR TREATING ALZHEIMER'S DISEASE OR HUNTINGTON'S DISEASE

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Page/Page column 13; 14; 35, (2020/03/23)

Benzimidazole compounds of formula (I), shown below, are disclosed. The compounds are potent human glutaminyl cyclase inhibitors. Also disclosed is a pharmaceutical composition containing one of these compounds and a pharmaceutical acceptable carrier, as well as a method of treating Alzheimer's disease or Huntington's disease by administering to a subject in need thereof an effective amount of such a compound.

BENZIMIDAZOLE COMPOUNDS AND USE THEREOF FOR TREATING ALZHEIMER'S DISEASE OR HUNTINGTON'S DISEASE

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Paragraph 0038; 0040; 0090-0091, (2020/03/23)

Benzimidazole compounds of formula (I), shown below, are disclosed. The compounds are potent human glutaminyl cyclase inhibitors. Also disclosed is a pharmaceutical composition containing one of these compounds and a pharmaceutical acceptable carrier, as well as a method of treating Alzheimer's disease or Huntington's disease by administering to a subject in need thereof an effective amount of such a compound.

HETEROCYCLIC COMPOUNDS AND USES THEREOF

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Paragraph 0145, (2020/10/21)

Heterocyclic compounds as Weel inhibitors are provided. The compounds may find use as therapeutic agents for the treatment of diseases and may find particular use in oncology.

ARTHROPOD PEST CONTROL METHOD EMPLOYING HETEROCYCLIC COMPOUND

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Paragraph 0331; 0335, (2019/12/28)

PROBLEM TO BE SOLVED: To provide an arthropod pest control method. SOLUTION: A compound represented by formula (I) in the figure or an N-oxide compound thereof is capable of controlling arthropod pests. [In the formula, Q represents a group represented by

HETEROCYCLE-SUBSTITUED TETRACYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR TREATMENT OF VIRAL DISEASES

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Page/Page column 128, (2014/08/06)

The present invention relates to novel Heterocycle-Substituted Tetracyclic Compounds of Formula (I): (I) and pharmaceutically acceptable salts thereof, wherein A, A', R 2 R 3, R 4 and R are as defined herein. The present i

THIAZOLYL-SUBSTITUED TETRACYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR TREATMENT OF VIRAL DISEASES

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Page/Page column 108, (2014/08/06)

The present invention relates to novel Thiazolyl-Substituted Tetracyclic Compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein A, A', R2R3, R4 and R5 are as defined herein. The present

Catalyst-controlled regioselective suzuki couplings at both positions of dihaloimidazoles, dihalooxazoles, and dihalothiazoles

Strotman, Neil A.,Chobanian, Harry R.,He, Jiafang,Guo, Yan,Dormer, Peter G.,Jones, Christina M.,Steves, Janelle E.

supporting information; experimental part, p. 1733 - 1739 (2010/05/18)

(Chemical Equation Presentation) Various dihaloazoles can be monoarylated at a single C-X bond with high selectivity via Suzuki coupling. By changing the palladium catalyst employed, the selectivity can be switched for some dihaloazoles, allowing for Suzuki coupling at the other, traditionally less reactive C-X bond. These conditions are applicable to coupling of a wide variety of aryl-, heteroaryl-, cyclopropyl-, and vinylboronic acids with high selectivities and enable the rapid construction of diverse arrays of diarylazoles in a modular fashion.

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