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3,5-Dichloro-4-thiocyanatoaniline is an organic compound with the chemical formula C7H4Cl2N2S. It is a derivative of aniline, where two chlorine atoms are attached to the 3rd and 5th carbon atoms, and a thiocyanate group is attached to the 4th carbon atom. This yellow crystalline solid is primarily used as a chemical intermediate in the synthesis of various dyes, pigments, and pharmaceuticals. Due to its reactive nature, it is essential to handle 3,5-Dichloro-4-thiocyanatoaniline with care, as it may pose health risks and environmental concerns.

7494-00-0

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7494-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7494-00-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7494-00:
(6*7)+(5*4)+(4*9)+(3*4)+(2*0)+(1*0)=110
110 % 10 = 0
So 7494-00-0 is a valid CAS Registry Number.

7494-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-amino-2,6-dichlorophenyl) thiocyanate

1.2 Other means of identification

Product number -
Other names I09-2147

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:7494-00-0 SDS

7494-00-0Downstream Products

7494-00-0Relevant academic research and scientific papers

Metal-Free and Visible-Light-Promoted C-3 Thiocyanation of 2-Arylquinolin-4-ones

Chauhan, Parul,Ritu,Preeti,Kumar, Sharvan,Jain, Nidhi

, p. 4334 - 4340 (2019/07/04)

A C-3 thiocyanation of 2-aryl-quinolin-4-ones in the presence of eosin-Y and visible light has been developed. The methodology allows easy access to a variety of 2-aryl-3-thiocyano-quinolin-4-ones in moderate to high yields. Regioselective para-thiocyanat

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