Welcome to LookChem.com Sign In|Join Free
  • or
2-Chloro-5-phenylthiazole is a chemical compound with the molecular formula C10H7ClS and a molecular weight of 197.68 g/mol. It is a thiazole derivative featuring a chlorine atom at position 2 and a phenyl group at position 5. 2-Chloro-5-phenylthiazole is recognized for its potential applications in various fields due to its unique structural properties.

329794-40-3

Post Buying Request

329794-40-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

329794-40-3 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Chloro-5-phenylthiazole is utilized as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new therapeutic agents. Its unique structure allows for the creation of a wide range of biologically active compounds, enhancing the diversity of available medications.
Used in Agrochemical Production:
In the agrochemical industry, 2-Chloro-5-phenylthiazole serves as an essential component in the production of various agrochemicals. Its incorporation aids in the development of effective solutions for pest and disease control in agriculture, ensuring crop protection and yield enhancement.
Used in Fine Chemicals Manufacturing:
2-Chloro-5-phenylthiazole is also employed in the manufacturing of fine chemicals, where its specific properties are leveraged to produce high-quality specialty chemicals for use in various industries, including fragrances, dyes, and other chemical intermediates.
Used in Antifungal and Antibacterial Applications:
2-Chloro-5-phenylthiazole has been studied for its potential antifungal and antibacterial properties, making it a promising candidate for the development of new therapeutic agents. Its ability to combat fungal and bacterial infections positions it as a valuable asset in the medical and pharmaceutical sectors, particularly in the creation of novel antimicrobial drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 329794-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,7,9 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 329794-40:
(8*3)+(7*2)+(6*9)+(5*7)+(4*9)+(3*4)+(2*4)+(1*0)=183
183 % 10 = 3
So 329794-40-3 is a valid CAS Registry Number.

329794-40-3SDS

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 2-chloro-5-phenyl-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 2-Chlor-4-phenylthiazol

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:329794-40-3 SDS

329794-40-3Relevant academic research and scientific papers

CYANOPYRROLIDINE DERIVATIVES WITH ACTIVITY AS INHIBITORS OF USP30

-

Page/Page column 57, (2018/06/16)

The present invention relates to a class of substituted-cyanopyrrolidines of Formula (I) with activity as inhibitors of deubiquitilating enzymes, in particular, ubiquitin C-terminal hydrolase 30 or ubiquitin specific peptidase 30 (USP30), having utility i

HETEROCYCLIC KINASE MODULATORS

-

Page/Page column 112, (2009/01/20)

The present disclosure provides heterocyclic protein kinase modulators and methods of using these compounds to treat diseases mediated by kinase activity.

Halogenated 2′-chlorobithiazoles via Pd-catalyzed cross-coupling reactions

Stanetty, Peter,Schnuerch, Michael,Mihovilovic, Marko D.

, p. 3754 - 3761 (2007/10/03)

Halogenated bithiazoles allow facile further functionalization and are, therefore, suitable intermediates for the synthesis of compounds with interesting biological activity or material science properties. The applicability of three coupling methods (Negi

Reactions With Heterocyclic Diazonium Salts. Synthesis of Several New Azolylhydrazones

Hafez, Ebtissam Abdel Aziz,Abed, Nosrat Mustafa,Elsakka, Ibrahim Ahmed

, p. 285 - 288 (2007/10/02)

Several new stable azolylhydrazones could be synthesized via coupling of diazotised cyclic amidines with active methylene reagents.The obtained compounds were utilised for synthesis of several, otherwise not readily accessible fused azoles.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 329794-40-3