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4-Benzothiazolecarbonitrile,2-amino-6-chloro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65948-26-7

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65948-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65948-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,4 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65948-26:
(7*6)+(6*5)+(5*9)+(4*4)+(3*8)+(2*2)+(1*6)=167
167 % 10 = 7
So 65948-26-7 is a valid CAS Registry Number.

65948-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-chloro-1,3-benzothiazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-benzothiazolecarbonitrile,2-amino-6-chloro

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:65948-26-7 SDS

65948-26-7Downstream Products

65948-26-7Relevant academic research and scientific papers

Synthesis and biological evaluation of novel N-pyridylpyrazolecarboxamides containing benzothiazole

Mao, Ming-Zhen,Wang, Hai-Yang,Wang, Wei,Ning, Bin-Ke,Li, Yu-Xin,Xiong, Li-Xia,Li, Zheng-Ming

, p. 42 - 46 (2016/12/24)

A series of novel N-pyridylpyrazolecarboxamides containing benzothiazolewere designed and synthesized. The target compounds were identified by 1H NMR,13C-NMR, IR, high-resolution mass spectrum (HRMS) and elemental analysis. The bioactivities of the newcom

Monoazo dyestuffs derived from benzothiazole

-

, (2008/06/13)

A disperse dye of the formula, STR1 wherein R1 is an alkyl group having 5 to 6 carbon atoms, R2 is an alkyl group having 5 to 6 carbon atoms, a cyano-ethyl group, R3 is a hydrogen atom or a lower alkyl, amino or phenyl group, and Y1 and Y2 represent independently a hydrogen atom, a lower alkyl group, a lower alkoxy group, a halogen atom, a nitro group, a cyano group, a thiocyanate group or an alkylsulfonyl group, provided that both Y1 and Y2 are not hydrogen at the same time and Y1 is located at the 4- or 5-position, which is useful for dyeing hydrophobic fibers in brilliant red to violet shade with good fastnesses.

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