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2-methyl-3-pyridyl tosylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1260000-13-2

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1260000-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1260000-13-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,0,0 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1260000-13:
(9*1)+(8*2)+(7*6)+(6*0)+(5*0)+(4*0)+(3*0)+(2*1)+(1*3)=72
72 % 10 = 2
So 1260000-13-2 is a valid CAS Registry Number.

1260000-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-3-pyridyl tosylate

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:1260000-13-2 SDS

1260000-13-2Relevant academic research and scientific papers

Copper-assisted preparation of pyridinyl sulfonate esters from hydroxypyridines and sodium sulfinates

Fan, Qiangwen,Le, Zhang-Gao,Li, Qian,Liu, Yishuai,Xie, Zongbo,Yang, Liu,Zhu, Haibo

, p. 2736 - 2740 (2022/02/09)

An efficient and powerful copper-assisted method for the effective conversion of a broad range of hydroxypyridines and sodium sulfinates into their corresponding pyridinyl tosylates was developed. Key features of this base- and ligand-free protocol include using the cheap and readily available CuBr2 as a medium and the use of sodium sulfinates as formal sulfonylation reagents. A variety of functional pyridinyl tosylates could be formed with good yields, which can easily be converted into C-C and C-N bond-containing compounds. This journal is

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