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152356-57-5

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152356-57-5 Usage

General Description

1-(6-Chloropyridin-2-yl)ethanone is a chemical compound with the molecular formula C7H6ClNO. It is a pale yellow liquid that is commonly used in the production of pharmaceuticals and agrochemicals. 1-(6-Chloropyridin-2-yl)ethanone is an important building block in organic synthesis, and it can undergo various chemical reactions to form more complex molecules. It is also used as a solvent and as an intermediate in the manufacture of dyes and flavors. 1-(6-Chloropyridin-2-yl)ethanone is considered to be a potentially hazardous chemical and should be handled with caution and proper safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 152356-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,3,5 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 152356-57:
(8*1)+(7*5)+(6*2)+(5*3)+(4*5)+(3*6)+(2*5)+(1*7)=125
125 % 10 = 5
So 152356-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO/c1-5(10)6-3-2-4-7(8)9-6/h2-4H,1H3

152356-57-5SDS

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 1-(6-CHLOROPYRIDIN-2-YL)ETHANONE

1.2 Other means of identification

Product number -
Other names -

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:152356-57-5 SDS

152356-57-5Relevant articles and documents

Visible-Light-Driven Direct Oxidative Coupling Reaction Leading to Alkyl Aryl Ketones, Catalyzed by Nano Pd/ZnO

Bazyar, Zahra,Hosseini-Sarvari, Mona

supporting information, p. 2282 - 2288 (2019/04/03)

Direct alkyl sp3 C–H activation to form new C–C bonds is one of the major challenges in synthetic chemistry. Herein, for the first time, we represent a new method, using nano Pd/ZnO which plays both as photoredox and transition-metal catalyst, for C–C bond formations. By using this catalyst, we have accomplished an oxidative coupling reaction between aryl halides and tertiary amines to yield the corresponding naturally occurring alkyl aryl ketones by using visible light irradiation. Furthermore, the carbonylation process was carried out on a 10 gram scale, with visible light and thermal condition, and it was proved to be scalable, efficient, and economical.

Ethanolamine derivatives having sympathomimetic and anti-pollakiuria activities

-

, (2008/06/13)

This invention relates to new ethanolamine derivatives having gut selective sympathomimetic and anti-pollakiuria activities and represented by the general formula [I]: STR1 wherein R1 is aryl or a heterocyclic group, each of which may be substituted with halogen, etc., R2 is hydrogen, halogen, nitro, hydroxy, lower alkyl optionally substituted with acyl, lower alkenyl optionally substituted with acyl, lower alkoxy optionally substituted with acyl, or amino optionally substituted with acyl(lower)alkyl, R3 is hydrogen, an N-protective group, or lower alkyl optionally substituted with lower alkylthio, n is an integer of 0 to 3, and a heavy solid line means a single bond or a double bond, provided that when n is 1, then 1) R1 is a condensed aromatic hydrocarbon group or a heterocyclic group, each of which may be substituted with halogen, etc., and the like, and pharmaceutically acceptable salts thereof to processes for the preparation thereof and to a pharmaceutical composition comprising the same.

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