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53544-69-7

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53544-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53544-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,4 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53544-69:
(7*5)+(6*3)+(5*5)+(4*4)+(3*4)+(2*6)+(1*9)=127
127 % 10 = 7
So 53544-69-7 is a valid CAS Registry Number.

53544-69-7SDS

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-(4-methylphenyl)-6-nitro-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 6-Nitro-2-p-tolyl-benzothiazol

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:53544-69-7 SDS

53544-69-7Downstream Products

53544-69-7Relevant articles and documents

Direct C-H arylation of benzothiazoles by magnetically separable nano copper ferrite, a recyclable catalyst

Satish,Reddy, K. Harsha Vardhan,Anil,Ramesh,Kumar, R. Uday,Nageswar

supporting information, p. 4950 - 4953 (2015/07/28)

Abstract A simple and highly practical method for the direct C-H arylation of benzothiazoles has been developed by using nano copper ferrite as a recyclable catalyst. The CuFe2O4 nano could be recovered and reused without significant loss of catalytic activity.

A highly efficient palladium-catalyzed desulfitative arylation of azoles with sodium arylsulfinates

Wang, Min,Li, Dengke,Zhou, Wei,Wang, Lei

experimental part, p. 1926 - 1930 (2012/03/26)

A highly efficient palladium-catalyzed direct desulfitative arylation of azoles at C2-position has been developed using sodium arylsulfinates as aryl sources. Azoles including benzoxazoles, benzothiazoles, oxazoles, thiazoles, and 1,3,4-oxadiazoles reacted with sodium arylsulfinates smoothly to generate the corresponding products in good to excellent yields, and various substitution patterns were tolerated toward the reaction.

Organic Phosphorus Compounds. 1. 4-(Benzothiazol-2-yl)benzylphosphonate as Potent Calcium Antagonistic Vasodilator

Yoshino, Kohichiro,Kohno, Toshihiko,Uno, Toshio,Morita, Tominori,Tsukamoto, Goro

, p. 820 - 825 (2007/10/02)

A series of 4-(benzothiazol-2-yl)benzylphosphonic acid dialkyl ester were synthesized and evaluated for coronary vasodilatory activity by Langendorff's method in the isolated guinea pig heart. Many of the phosphonic acid dialkyl esters exhibited vasodilat

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