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N-(2-iodophenyl)-N-phenylacetamide is an organic compound with the chemical formula C14H12INO. It is a derivative of acetamide, featuring a 2-iodophenyl group attached to the nitrogen atom, and a phenyl group attached to the other nitrogen atom. N-(2-iodophenyl)-N-phenylacetamide is characterized by its molecular weight of 355.16 g/mol and a melting point of 150-152°C. It is a white to off-white crystalline solid and is soluble in common organic solvents such as ethanol, methanol, and acetone. N-(2-iodophenyl)-N-phenylacetamide is primarily used in the synthesis of pharmaceuticals and as an intermediate in the preparation of various chemical compounds. Due to its potential applications in the medical field, it is essential to understand its chemical properties and reactivity to ensure safe handling and use.

2236-45-5

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2236-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2236-45-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,3 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2236-45:
(6*2)+(5*2)+(4*3)+(3*6)+(2*4)+(1*5)=65
65 % 10 = 5
So 2236-45-5 is a valid CAS Registry Number.

2236-45-5Downstream Products

2236-45-5Relevant academic research and scientific papers

Aryl halide tolerated electrophilic amination of arylboronic acids with N-chloroamides catalyzed by CuCl at room temperature

He, Chuan,Chen, Chong,Cheng, Jin,Liu, Chao,Liu, Wei,Li, Qiang,Lei, Aiwen

supporting information; experimental part, p. 6414 - 6417 (2009/03/11)

(Chemical Equation Presented) N-Cl is no competition: Aryl halides were tolerated in an efficient ligandless CuCl-catalyzed electrophilic amination reaction of arylboronic acids with N-chloroamides (see scheme; Ac=acetoxy). This coupling proceeded smoothly at ambient temperature, and products were obtained with good to excellent yields.

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