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136592-10-4

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136592-10-4 Usage

General Description

Ethanone, 2-chloro-1-[6-(methylthio)-3-pyridinyl]- (9CI) is a chemical compound that is also known by its chemical names 2-chloro-1-(6-(methylthio)pyridin-3-yl)ethan-1-one or 2-chloro-1-(6-(methylsulfanyl)pyridin-3-yl)ethan-1-one. It is a chlorinated derivative of pyridine and is used in the synthesis of various pharmaceuticals and agrochemicals. Ethanone, 2-chloro-1-[6-(methylthio)-3-pyridinyl]- (9CI) has potential use in the field of medicinal chemistry due to its structural properties and activities against certain biological targets. However, it is important to handle this chemical with care as it may have hazardous properties and should be used in a controlled laboratory environment.

Check Digit Verification of cas no

The CAS Registry Mumber 136592-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,9 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136592-10:
(8*1)+(7*3)+(6*6)+(5*5)+(4*9)+(3*2)+(2*1)+(1*0)=134
134 % 10 = 4
So 136592-10-4 is a valid CAS Registry Number.

136592-10-4SDS

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-1-(6-methylsulfanylpyridin-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2-CHLORO-1-[6-(METHYLTHIO)-3-PYRIDINYL]-ETHANONE

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:136592-10-4 SDS

136592-10-4Downstream Products

136592-10-4Relevant articles and documents

The chemistry of pseudomonic acid part 14. Synthesis and in vivo biological activity of heterocyclyl substituted oxazole derivatives

Broom,Elder,Hannan,Pons,O'Hanlon,Walker,Wilson,Woodall

, p. 1336 - 1344 (2007/10/02)

Semisynthetic analogues of pseudomonic acid A have been prepared containing a heterocyclyl substituted oxazole. Derivatives in which the heterocycle was thiophene, furan, pyridine, or isoxazole showed good antibacterial potency and were further evaluated in vivo. Both pharmacokinetic parameters and oral activity against an experimental intraperitoneal sepsis were superior to results obtained from previously described pseudomonic acid A derivatives.

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