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5-Methyl-2-(methylthio)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51933-75-6

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51933-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51933-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,3 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51933-75:
(7*5)+(6*1)+(5*9)+(4*3)+(3*3)+(2*7)+(1*5)=126
126 % 10 = 6
So 51933-75-6 is a valid CAS Registry Number.

51933-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2-(methylsulfanyl)pyridine

1.2 Other means of identification

Product number -
Other names 5-methyl-2-methylsulfanyl-pyridine

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:51933-75-6 SDS

51933-75-6Downstream Products

51933-75-6Relevant academic research and scientific papers

Cesium carbonate-promoted synthesis of aryl methyl sulfides using: S -methylisothiourea sulfate under transition-metal-free conditions

Zhang, Caiyang,Zhou, You,Huang, Jintao,Tu, Canhui,Zhou, Xiaoai,Yin, Guodong

, p. 6316 - 6321 (2018/09/10)

In the presence of cesium carbonate, an efficient synthesis of aryl methyl sulfides by the reactions of aryl halides with commercially available S-methylisothiourea sulfate is developed. This odourless and highly crystalline solid can be used as the subst

Complex-induced proximity effect in the regioselective lithiation of pyridine derivatives

Dhau, Jaspreet S.,Singh, Amritpal,Kasetti, Yoganjaneyulu,Bharatam

, p. 1746 - 1752 (2012/05/04)

The regioselective ring lithiation of BF3-complexed 3-picoline (1a), 3,4-lutidine (1b), and 3,5-lutidine (1c) was studied. The dilithiation of 1a, 1b, and 1c was also investigated to experimentally explore the relative preference of the sites on the substituted pyridine ring for lithiation. The role of the complex-induced proximity effect (CIPE) for inducing lithiation in these moieties was investigated using both experimental and computational studies.

Unprecedented C-6 functionalisation of 3-picoline induced by a methyl to C-6 lithium shift

Mathieu, Julien,Gros, Philippe,Fort, Yves

, p. 951 - 952 (2007/10/03)

BuLi-Me2N(CH2)2OLi (BuLi-LiDMAE) promoted the clean C-6 functionalisation of 3-picoline via a methyl to C-6 lithium shift.

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