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Pent-2-enanilide, also known as 2-pentylbenzamide, is an organic compound with the chemical formula C12H17NO. It is a derivative of benzamide, where a pentyl group (C5H11) is attached to the para position of the benzene ring. pent-2-enanilide is characterized by its amide functional group, which consists of a carbonyl group (C=O) bonded to a nitrogen atom (N). Pent-2-enanilide is a colorless to pale yellow solid with a melting point of approximately 40-42°C. It is soluble in organic solvents such as ethanol, acetone, and dichloromethane, but has limited solubility in water. This chemical can be synthesized through various methods, including the reaction of 2-pentylbenzoic acid with ammonia or amines. Pent-2-enanilide has potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various drugs and other organic compounds.

1483-35-8

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1483-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1483-35-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1483-35:
(6*1)+(5*4)+(4*8)+(3*3)+(2*3)+(1*5)=78
78 % 10 = 8
So 1483-35-8 is a valid CAS Registry Number.

1483-35-8Relevant academic research and scientific papers

Low-Valent Tungsten Catalysis Enables Site-Selective Isomerization-Hydroboration of Unactivated Alkenes

Cooper, Phillippa,Engle, Keary M.,Jankins, Tanner C.,Martin, Ruben,Martin-Montero, Raul

supporting information, p. 14981 - 14986 (2021/09/29)

A tungsten-catalyzed hydroboration of unactivated alkenes at distal C(sp3)-H bonds aided by native directing groups is described herein. The method is characterized by its simplicity, exquisite regio- and chemoselectivity, and wide substrate scope, offering a complementary site-selectivity pattern to other metal-catalyzed borylation reactions and chain-walking protocols.

Copper-catalyzed oxidative amidation between aldehydes and arylamines under mild conditions

Ding, Yongzheng,Zhang, Xian,Zhang, Dongyang,Chen, Yuting,Wu, Zhibing,Wang, Peiyi,Xue, Wei,Song, Baoan,Yang, Song

supporting information, p. 831 - 833 (2015/02/19)

A facile strategy to prepare amide bonds has been developed. A series of amide compounds, including heterocyclic amide compounds, were obtained with moderate to good yields ranging from 31-88% by using copper iodide (CuI) to catalyze the oxidative amidation between aldehydes and amines under solvent-free conditions at room temperature in air.

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