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3-(2-chlorophenyl)prop-2-ynamide is an organic compound with the chemical formula C9H6ClNO. It is a derivative of prop-2-ynamide, featuring a 2-chlorophenyl group attached to the third carbon atom. 3-(2-chlorophenyl)prop-2-ynamide is characterized by its unique structure, which includes a triple bond between the second and third carbon atoms, and a chlorine atom attached to the ortho position of the phenyl ring. It is a colorless solid with a molecular weight of 177.60 g/mol. Due to its reactivity and the presence of a triple bond, it can be used as a building block in the synthesis of various organic compounds, particularly those involving the formation of carbon-carbon bonds. The compound's properties, such as its reactivity and potential applications, make it an interesting subject for research in organic chemistry and material science.

3533-13-9

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3533-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3533-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3533-13:
(6*3)+(5*5)+(4*3)+(3*3)+(2*1)+(1*3)=69
69 % 10 = 9
So 3533-13-9 is a valid CAS Registry Number.

3533-13-9Relevant academic research and scientific papers

MODULATORS OF CASPASE-6

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Paragraph 000109-000115, (2016/04/26)

The current application relates to a pharmaceutical composition for the treatment or amelioration of a neurological disease, wherein the composition comprises a therapeutically effective amount of a caspase-6 inhibitor which is an arylpropynamide derivative. The composition can be formulated for oral or topical administration, subcutaneous, intravenous, or intramuscular injection, infusion, inhalation, or intrthecal injection.

Preparation of arylpropynamides and their reaction with malonyl acid derivatives

Petina, Olgaa. A.,Yakovlev, Igorp. P.,Geffken, Detlef

, p. 803 - 809 (2013/04/10)

Synthesis of arylpropynamides and their reactions with different malonic acid derivatives is described. Treatment of arylpropynamides with unsubstituted malonyl chloride furnished N-(3-arylprop-2-ynoyl)-6-chloro-4-hydroxy-2-oxo-2H- pyran-3-carboxamides; m

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