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2,4-Pentadienethioamide, 3-amino-N,N-dimethyl-5-phenylis a chemical compound characterized by the molecular formula C12H16N2S. It is a thioamide derivative featuring a 2,4-pentadiene backbone and a substituent that includes an amino group, two methyl groups, and a phenyl group. 2,4-Pentadienethioamide, 3-amino-N,N-dimethyl-5-phenylholds potential in medicinal chemistry and pharmaceutical research, possibly exhibiting biological activities or serving as a precursor for the synthesis of other organic molecules. Further investigation is required to comprehensively understand its properties and potential applications.

156366-79-9

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156366-79-9 Usage

Uses

Used in Pharmaceutical Research:
2,4-Pentadienethioamide, 3-amino-N,N-dimethyl-5-phenylis used as a potential building block for the synthesis of other organic molecules in pharmaceutical research. Its unique structure may contribute to the development of new drugs or therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,4-Pentadienethioamide, 3-amino-N,N-dimethyl-5-phenylis utilized for exploring its potential biological activities. These activities could lead to the discovery of new compounds with therapeutic potential, further expanding the scope of available treatments for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 156366-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,6 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156366-79:
(8*1)+(7*5)+(6*6)+(5*3)+(4*6)+(3*6)+(2*7)+(1*9)=159
159 % 10 = 9
So 156366-79-9 is a valid CAS Registry Number.

156366-79-9Downstream Products

156366-79-9Relevant academic research and scientific papers

Synthesis of 3-Aminothiophene-2-thioamides

Auer,Weis,Schweiger

, p. 1027 - 1030 (1996)

4-Dimethylamino-5,6-dihydro-2H-thiopyran-2-thiones (1) were alkylated to N,N-dimethyl-6-methylthio-2H-thiopyran-4(3H)-iminiumiodides(2). Aminolysis of the latter with ammonia led to 6-dimethylamino-2H-thiopyran-4(3H)-iminiumiodides (3) which were hydrolyz

Syntheses of 5-dialkylamino-1,2-oxazoles from N,N-dialkyl-β-amino-α,β,γ,δ-unsaturated thioamides

Auer, H.,Weis, R.,Schweiger, K.,Schubert-Zsilavecz, M.

, p. 571 - 578 (2007/10/02)

3-Amino-2,4-pentadienthioamides, which were obtained from 6-dialkylamino-2H-thiopyrane-4(3H)iminium halides by alkali hydrolysis, react with hydroxylamine hydrochloride in a +-addition to give selectively 5-amino-3-alkenyl-1,2-oxazoles.These o

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