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2,3-Dichloro-4-thiocyanatoaniline is a chemical compound characterized by its molecular formula C6H4Cl2N2S. It presents as a yellow to brown crystalline solid, notable for its strong coloration properties, which make it a valuable intermediate in the synthesis of dyes and pigments.

7494-03-3

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7494-03-3 Usage

Uses

Used in Dye and Pigment Synthesis:
2,3-Dichloro-4-thiocyanatoaniline is used as an intermediate in the production of various dyes and pigments, due to its strong coloration capabilities.
Used in Hair Dye Manufacturing:
In the cosmetics industry, 2,3-Dichloro-4-thiocyanatoaniline is used as a colorant in hair dyes, contributing to their vibrant and long-lasting hues.
Used in Textile Industry:
2,3-Dichloro-4-thiocyanatoaniline is utilized in the textile industry as a dyeing agent, enhancing the colorfastness and visual appeal of fabrics.
Used in Paint Production:
2,3-Dichloro-4-thiocyanatoaniline is employed in the paint industry to provide intense colors and improve the durability of the paint.
Used in Biochemical Research:
In the field of biochemical research, 2,3-Dichloro-4-thiocyanatoaniline serves as a reagent for detecting the presence of specific enzymes and proteins, owing to its unique chemical properties.
Caution:
Given its toxic properties, 2,3-Dichloro-4-thiocyanatoaniline should be handled with care to ensure safety in all applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7494-03-3 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 7494-03:
(6*7)+(5*4)+(4*9)+(3*4)+(2*0)+(1*3)=113
113 % 10 = 3
So 7494-03-3 is a valid CAS Registry Number.

7494-03-3SDS

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-2,3-dichlorophenyl) thiocyanate

1.2 Other means of identification

Product number -
Other names 2,3-Dichloro-4-thiocyanato-phenylamine

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:7494-03-3 SDS

7494-03-3Relevant academic research and scientific papers

Kepner-Tregoe Decision Analysis as a tool to aid route selection. Part 3. Application to a back-up series of compounds in the PDK project

Parker, Jeremy S.,Bower, John F.,Murray, Paul M.,Patel, Bharti,Talavera, Pere

, p. 1060 - 1077 (2013/01/03)

Kepner-Tregoe Decision Analysis was used to rank 22 potential routes to a back-up series of compounds in the PDK project. The ten highest scoring routes were evaluated practically, affording four new synthetic sequences for preparing the target compounds.

Substituted N-phenyl 2-hydroxy-2-methyl-3,3,3-trifluoropropanamide derivatives which elevate pyruvate dehydrogenase activity

-

Page column 55, (2010/02/05)

A compound of formula (I) wherein: n is 1 or 2; R 1 is chloro, fluoro, bromo, methyl or methoxy; R 2 is as defined within; R 3 is as defined within; and R 4 is hydrogen or fluoro; or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof is described. The use of compounds of formula (I) in the production of an elevation of PDH activity in a warm-blooded animal such as a human being are also described. Pharmaceutical compositions, methods and processes for preparation of compounds of formula (I) are detailed. STR1

Substituted-4-alkylthioalkane-sulfonanilides and operatives

-

, (2008/06/13)

Alkane- and monohaloalkane-sulfonanilides substituted in the para position by alkylthio, alkylsulfinyl and alkylsulfonyl groups and additionally substituted by halogen and optionally by trifluoromethyl and agriculturally acceptable salts thereof are useful herbicides.

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