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1-(pyridin-2-ylsulfanyl)propan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3166-26-5

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3166-26-5 Usage

Appearance

Yellow liquid

Molecular weight

167.23 g/mol

Usage

Building block in organic synthesis

Application in

Pharmaceutical and agrochemical production

Industrial applications

Development of new materials

Pharmacological properties

Inhibition of certain enzymes

Potential activity

Antifungal activity

Fields of application

Chemistry, pharmaceuticals, and materials science

Check Digit Verification of cas no

The CAS Registry Mumber 3166-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3166-26:
(6*3)+(5*1)+(4*6)+(3*6)+(2*2)+(1*6)=75
75 % 10 = 5
So 3166-26-5 is a valid CAS Registry Number.

3166-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pyridin-2-ylsulfanylpropan-2-one

1.2 Other means of identification

Product number -
Other names 1-(pyridin-2-ylsulfanyl)propan-2-one

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:3166-26-5 SDS

3166-26-5Downstream Products

3166-26-5Relevant academic research and scientific papers

Synthesis of α-arylthioacetones using TEMPO as the: C 3 synthon via a reaction cascade of sequential oxidation, skeletal rearrangement and C-S bond formation

Zou, Jiao-Xia,Jiang, Yi,Lei, Shuai,Yin, Gao-Feng,Hu, Xiao-Ling,Zhao, Quan-Yi,Wang, Zhen

supporting information, p. 2341 - 2345 (2019/03/07)

Here, we present an unprecedented pathway to α-sulfenylated carbonyl compounds from commercially available thiols and universally employed TEMPO and its analogues, which act as C3 synthons through skeletal rearrangement under simple and metal-f

Kinetic resolution of heteroaryl β-hydroxy sulfides catalyzed by Humicola lanuginosa lipase

Chimni, Swapandeep Singh,Singh, Satwinder,Kumar, Subodh,Mahajan, Savita

, p. 511 - 517 (2007/10/03)

Humicola lanuginosa lipase-catalyzed resolution of heteroaryl substituted β-hydroxy sulfides by irreversible transesterification using vinyl acetate as acylating agent is discussed. The ee of the resolved alcohols was determined from the 1H NMR of their corresponding (S)-(+)-O-acetylmandelic acid esters.

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