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5-METHOXY-2-(2-PYRIDYL)BENZOTHIAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39876-33-0

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39876-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39876-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,7 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39876-33:
(7*3)+(6*9)+(5*8)+(4*7)+(3*6)+(2*3)+(1*3)=170
170 % 10 = 0
So 39876-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2OS/c1-16-9-5-6-12-11(8-9)15-13(17-12)10-4-2-3-7-14-10/h2-8H,1H3

39876-33-0SDS

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 5-methoxy-2-pyridin-2-yl-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 5-methoxy-2-(pyridin-2-yl)-1,3-benzothiazole

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:39876-33-0 SDS

39876-33-0Downstream Products

39876-33-0Relevant academic research and scientific papers

Functionalization of primary ch bonds in picolines toward pyridylthioamides

Ho, Tuan H.,Le, Ha H. K.,Nguyen, Tung T.,Phan, Nam T. S.,To, Tuong A.

, p. 783 - 789 (2020/08/28)

We report a method for coupling of nitroarenes, 2- or 4-methylazaarenes, and elemental sulfur to afford (2-pyridyl)aryl thioamides. Good tolerance of functionalities was observed, including primary and secondary amines, bromo, iodo, ester, and boronic est

Nitro-methyl redox coupling: Efficient approach to 2-hetarylbenzothiazoles from 2-halonitroarene, methylhetarene, and elemental sulfur

Nguyen, Thanh Binh,Ermolenko, Ludmila,Al-Mourabit, Ali

supporting information, p. 4218 - 4221 (2013/09/12)

A simple, straightforward, and atom economic approach to 2-hetarylbenzothiazoles starting from 2-halonitroarene, methylhetarene, and elemental sulfur under mild conditions is described. The method is highlighted by the direct redox nitro-methyl reaction for carbon-nitrogen bond formation without an added oxidizing or reducing agent.

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