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N,N-dimethyl-2,4-dithiocyanatoaniline is an organic compound with the chemical formula C9H10N2S2. It is a derivative of aniline, where two hydrogen atoms on the nitrogen are replaced by methyl groups, and the two hydrogen atoms on the ortho and para positions of the benzene ring are replaced by dithiocyanato groups. N,N-dimethyl-2,4-dithiocyanatoaniline is known for its reactivity and is used in the synthesis of various dyes and pigments. It is also recognized for its potential applications in the field of materials science, particularly in the development of conductive polymers and other specialized chemical products. Due to its reactivity, it is important to handle N,N-dimethyl-2,4-dithiocyanatoaniline with care, following appropriate safety protocols.

7494-05-5

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7494-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7494-05-5 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 7494-05:
(6*7)+(5*4)+(4*9)+(3*4)+(2*0)+(1*5)=115
115 % 10 = 5
So 7494-05-5 is a valid CAS Registry Number.

7494-05-5Downstream Products

7494-05-5Relevant academic research and scientific papers

A versatile procedure for the preparation of aryl thiocyanates using N-thiocyanatosuccinimide (NTS)

Toste,De Stefano,Still

, p. 1277 - 1286 (1995)

A mild procedure for the thiocyanation of several types of arene substrate using N-thiocyanatosuccinimide (NTS) is described. The method appears generally applicable to benzenoid substrates with a wide range of substituents, as well as to heteroaromatic a

Electrochemical ipso-Thiocyanation of Arylboron Compounds

Dyga, Marco,Hayrapetyan, Davit,Rit, Raja K.,Goo?en, Lukas J.

supporting information, p. 3548 - 3553 (2019/04/26)

An operationally simple electrochemical method for the transition-metal-free ipso-thiocyanation of arylboronic acids and aryl trifluoroborates has been developed. The SCN electrophile is generated in situ by anodic oxidation of thiocyanate anions, which avoids formation of salt waste and prevents unwanted side reactions arising from chemical oxidants. The reaction proceeds regiospecifically, and the scope extends to non-activated aromatic systems. (Figure presented.).

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