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Propan-2-yl (2-chlorophenyl)carbamate is a chemical compound with the molecular formula C10H12ClNO2. It is an ester derivative of carbamic acid, where the hydroxyl group is replaced by a propyl group and a 2-chlorophenyl group. propan-2-yl (2-chlorophenyl)carbamate is characterized by its potential reactivity due to the presence of the carbamate functional group, which can undergo hydrolysis in the presence of water to form an amine and carbon dioxide. The 2-chlorophenyl group introduces a chlorine atom at the ortho position, which may affect the compound's reactivity and physical properties. Propan-2-yl (2-chlorophenyl)carbamate is typically used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, owing to its ability to form stable derivatives with other functional groups. Its specific applications and properties are determined by the nature of the substituents and the reactions it undergoes, making it a versatile building block in organic chemistry.

2150-22-3

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2150-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2150-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2150-22:
(6*2)+(5*1)+(4*5)+(3*0)+(2*2)+(1*2)=43
43 % 10 = 3
So 2150-22-3 is a valid CAS Registry Number.

2150-22-3Downstream Products

2150-22-3Relevant academic research and scientific papers

Reactions of Primary and Secondary Amines with Fluoronitrene Generated from Isopropyl N,N-Difluorocarbamate

Klopotek, David L.,Hobrock, Brice G.,Kovacic, Peter,Jones, Martin B.

, p. 1665 - 1667 (2007/10/02)

Isopropyl N,N-difluorocarbamate deaminates primary amines, RNH2, affording RH, N2, RNHCO2-i-C3H7, and RNH2*HF.With secondary amines, dibenzylamine gives bibenzyl, whereas pyrrolidine yields a ring-expansion product, 2,3,4,5-tetrahydropyridazine.The reactions are consistent with the generation of fluoronitrene and subsequent production of the intermediates RN=NH from RNH2 and R2N=N from R2NH.The advantages of using isopropyl N,N-difluorocarbamate as a source of fluoronitrene are discussed.

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