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148637-74-5

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148637-74-5 Usage

General Description

5-Thiazolecarbonyl chloride, 2-chloro- (9CI) is a chemical compound that belongs to the thiazolecarbonyl chloride family. It is a colorless or light yellow clear liquid with a pungent odor. 5-Thiazolecarbonyl chloride, 2-chloro- (9CI) is primarily used as a reagent in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is a versatile intermediate that can be used in the synthesis of various thiazole-containing compounds, which have applications in the fields of medicine and agriculture. Additionally, it can also be used as an intermediate in the production of dyes and pigments. However, it is important to handle this compound with caution as it is corrosive and can cause irritation to the skin, eyes, and respiratory system upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 148637-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,6,3 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 148637-74:
(8*1)+(7*4)+(6*8)+(5*6)+(4*3)+(3*7)+(2*7)+(1*4)=165
165 % 10 = 5
So 148637-74-5 is a valid CAS Registry Number.
InChI:InChI=1/C4HCl2NOS/c5-3(8)2-1-7-4(6)9-2/h1H

148637-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1,3-thiazole-5-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 5-Thiazolecarbonylchloride,2-chloro

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:148637-74-5 SDS

148637-74-5Relevant articles and documents

VECTOR CONTROL COMPOSITIONS, METHODS AND PRODUCTS UTILIZING SAME

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Page/Page column 42; 43; 44, (2019/05/15)

The present inventions concerns use of a specific methoxyacrylate compound to control mosquitoes, and vector control products comprising that methoxyacrylate compound, in particular the invention relates to a substrate, to a composition, for controlling mosquitoes, and to a specific methoxyacrylate compound, processes for the synthesis of mosquitocidal methoxyacrylate compounds and new intermediates.

Small molecule disruptors of the glucokinase-glucokinase regulatory protein interaction: 3. Structure-activity relationships within the aryl carbinol region of the N-arylsulfonamido-N′-arylpiperazine series

Nishimura, Nobuko,Norman, Mark H.,Liu, Longbin,Yang, Kevin C.,Ashton, Kate S.,Bartberger, Michael D.,Chmait, Samer,Chen, Jie,Cupples, Rod,Fotsch, Christopher,Helmering, Joan,Jordan, Steven R.,Kunz, Roxanne K.,Pennington, Lewis D.,Poon, Steve F.,Siegmund, Aaron,Sivits, Glenn,Lloyd, David J.,Hale, Clarence,St. Jean, David J.

, p. 3094 - 3116 (2014/05/06)

We have recently reported a novel approach to increase cytosolic glucokinase (GK) levels through the binding of a small molecule to its endogenous inhibitor, glucokinase regulatory protein (GKRP) these initial investigations culminated in the identification of 2-(4-((2S)-4-((6-amino-3- pyridinyl)sulfonyl)-2-(1-propyn-1-yl)-1-piperazinyl)phenyl)-1,1,1,3,3, 3-hexafluoro-2-propanol (1, AMG-3969), a compound that effectively enhanced GK translocation and reduced blood glucose levels in diabetic animals. Herein we report the results of our expanded SAR investigations that focused on modifications to the aryl carbinol group of this series. Guided by the X-ray cocrystal structure of compound 1 bound to hGKRP, we identified several potent GK-GKRP disruptors bearing a diverse set of functionalities in the aryl carbinol region. Among them, sulfoximine and pyridinyl derivatives 24 and 29 possessed excellent potency as well as favorable PK properties. When dosed orally in db/db mice, both compounds significantly lowered fed blood glucose levels (up to 58%).

HETEROCYCLIC AMINOBERBAMINE DERIVATIVES, THE PREPARATION PROCESS AND USE THEREOF

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Paragraph 0108, (2013/07/19)

The present invention relates to a novel berbamine derivative of formula I or a pharmaceutically acceptable salt thereof, a process for preparation of the same, a pharmaceutical composition comprising said compound and its use in manufacture of an antitumor medicament.

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