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Hexyl (3-chlorophenyl)carbamate is a chemical compound with the molecular formula C13H16ClNO2. It is an organocarbamate, which is a type of carbamic acid ester formed by the reaction of an alcohol and a carbamic acid. In this case, the alcohol is hexanol, and the carbamic acid is derived from 3-chlorophenol. hexyl (3-chlorophenyl)carbamate is characterized by its potential use as an insecticide, due to the carbamate group's ability to inhibit acetylcholinesterase, an enzyme crucial for nerve impulse transmission in insects. The presence of the 3-chlorophenyl group may contribute to its specific mode of action or target pests. It is important to note that the use of such chemicals must be managed carefully due to their potential environmental and health impacts, and they are subject to regulatory controls to ensure safe application.

2150-90-5

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2150-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2150-90-5 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, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2150-90:
(6*2)+(5*1)+(4*5)+(3*0)+(2*9)+(1*0)=55
55 % 10 = 5
So 2150-90-5 is a valid CAS Registry Number.

2150-90-5Downstream Products

2150-90-5Relevant academic research and scientific papers

Efficient preparation of carbamates by Rh-catalysed oxidative carbonylation: unveiling the role of the oxidant

Iturmendi, Amaia,Iglesias, Manuel,Munárriz, Julen,Polo, Victor,Pérez-Torrente, Jesús J.,Oro, Luis A.

, p. 404 - 407 (2017)

The synthesis of a wide variety of carbamates from amines, alcohols and carbon monoxide has been achieved by means of a Rh-catalysed oxidative carbonylation reaction that uses Oxone as a stoichiometric oxidant. In-depth studies on the reaction mechanism shed light on the intimate role of Oxone in the catalytic cycle.

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