82613-35-2 Usage
Chemical structure
A benzene ring with two attached carbothioamide groups and two sulfonyl groups attached to the amide nitrogen atoms.
Functional groups
Carbothioamide and sulfonyl groups.
Industrial applications
a. Intermediate in the synthesis of pharmaceuticals.
b. Building block in the production of organic materials.
Reactivity
The presence of carbothioamide and sulfonyl groups makes the compound useful for forming new chemical bonds and interacting with other molecules in a controlled manner.
Versatility
Potential applications in synthetic chemistry and materials science.
Molecular weight
Approximately 370.50 g/mol (calculated from the molecular formula).
Appearance
The compound is likely to be a solid, although the specific appearance (e.g., color, crystal structure) is not provided in the material.
Stability
The stability of the compound is not explicitly mentioned in the material, but the presence of multiple functional groups suggests that it may be sensitive to certain reaction conditions.
Hazards
The material does not provide information on the hazards associated with 1,2-Benzenedicarbothioamide,N1,N2-bis[(4-methylphenyl)sulfonyl]-, but it is important to consider potential hazards when handling chemicals, such as toxicity, flammability, or reactivity with other substances.
Check Digit Verification of cas no
The CAS Registry Mumber 82613-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,1 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82613-35:
(7*8)+(6*2)+(5*6)+(4*1)+(3*3)+(2*3)+(1*5)=122
122 % 10 = 2
So 82613-35-2 is a valid CAS Registry Number.
82613-35-2Relevant academic research and scientific papers
Reaction of N,N'-Di(p-tolylsulphonyl)phthaldithioamide with Amines
El-Sharief, A. M. Sh.,Mekky, A. K. T.,Yousef, A. A.
, p. 245 - 247 (2007/10/02)
The dithiophthalamide (II) on alkylation with ethyl sulphate gives the corresponding N,N'-diethyl derivative (III), while its reaction with HgCl2, S-benzylisothiouronium chloride and one or two mol of amines in acetic acid gives IV, V and the mono-(VI) or di-imino (VIII) derivatives, respectively.Action of semicarbazide, hydrazines or other amines on II in ethanol results in the replacement of one or both the sulphonamido groups with the amine used to give IX or X respectively.Reactions of II with benzylamine, aniline and copper turnings have also been studied.
