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Hydrazinecarbothioamide, 2-[(2,4,6-trimethylphenyl)methylene]-, also known as 2-[(2,4,6-trimethylphenyl)methylene]hydrazinecarbothioamide, is an organic compound with the chemical formula C11H14N2S. It is a derivative of hydrazinecarbothioamide, featuring a 2,4,6-trimethylphenyl group attached to the methylene bridge. Hydrazinecarbothioamide, 2-[(2,4,6-trimethylphenyl)methylene]- is characterized by its unique structure, which includes a hydrazine group, a carbonyl group, and a thioamide group, all connected to a trimethylphenyl ring. It is primarily used in chemical research and synthesis, particularly in the development of pharmaceuticals and other organic compounds. Due to its complex structure, it is essential to handle this chemical with care, adhering to proper safety protocols and regulations.

3383-16-2

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3383-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3383-16-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3383-16:
(6*3)+(5*3)+(4*8)+(3*3)+(2*1)+(1*6)=82
82 % 10 = 2
So 3383-16-2 is a valid CAS Registry Number.

3383-16-2Downstream Products

3383-16-2Relevant academic research and scientific papers

Facile synthesis and biological assays of novel 2,4-disubstituted hydrazinyl-thiazoles analogs

Ghanbari Pirbasti, Fateme,Mahmoodi, Nosrat O.

, p. 497 - 506 (2016/04/20)

A convenient, one-pot multi-component synthesis of new 2,4-disubstituted hydrazinyl-thiazoles was accomplished using different aldehydes/ketones, thiosemicarbazide, and 4-methoxy phenacyl bromide in the presence of a catalytic amount of AcOH in EtOH. Prod

Synthesis of 2-amino-1,3,4-oxadiazoles and 2-Amino-1,3,4-thiadiazoles via sequential condensation and I2-mediated oxidative C-O/C-S bond formation

Niu, Pengfei,Kang, Jinfeng,Tian, Xianhai,Song, Lina,Liu, Hongxu,Wu, Jie,Yu, Wenquan,Chang, Junbiao

, p. 1018 - 1024 (2015/01/30)

2-Amino-substituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles were synthesized via condensation of semicarbazide/thiosemicarbazide and the corresponding aldehydes followed by I2-mediated oxidative C-O/C-S bond formation. This transition-metal-free sequential synthesis process is compatible with aromatic, aliphatic, and cinnamic aldehydes, providing facile access to a variety of diazole derivatives bearing a 2-amino substituent in an efficient and scalable fashion.

Reactions of trichloromethylarenes with hydrazine derivatives. Synthesis of 2,5-disubstituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles

Poddubnyi,Belen'kii,Krayushkin

, p. 1185 - 1188 (2007/10/03)

The effect of the solvent on the course of the reaction between trichloromethylarenes and thioacylhydrazines or acylhydrazines has been considered. In alcohols as solvents, alkyl arenecarboxylates form as a result of alcoholysis, while 2,5-disubstituted 1,3,4-thiadiazoles (1,3,4-oxadiazoles) form as minor products. In pyridine solutions, the major or sole products are those of reductive condensation, i.e., the corresponding N-substituted hydrazones of arenecarbaldehydes. 1,3,4-Thiadiazole or 1,3,4-oxadiazole derivatives are obtained in good yield when the reaction is carried out in a pyridine - alkanol mixture.

SYNTHESIS OF 2-AMINO-5-ARYL-1,3,4-THIADIAZOLES FROM TRICHLOROMETHYLARENES: THE EFFECT OF REACTION CONDITIONS

Belen'kii, Leonid,Poddubny, Igor,Krayushkin, Mikhaill

, p. 469 - 470 (2007/10/02)

The factors have been considered controlling the course of the interaction between trichloromethylarenes and thioacylhydrazines.

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