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N-(Chloroformyl)cyclohexylamine is a chemical compound with the molecular formula C7H12ClNO. It is a derivative of cyclohexylamine, where the hydrogen atom in the formyl group (CHO) is replaced by a chlorine atom. N-(Chloroformyl)cyclohexylamine is primarily used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It is known for its ability to react with amines, alcohols, and other nucleophiles, forming valuable intermediates in the synthesis of complex molecules. Due to its reactivity, it is important to handle N-(Chloroformyl)cyclohexylamine with care, as it can be toxic and hazardous.

4363-92-2

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4363-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4363-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4363-92:
(6*4)+(5*3)+(4*6)+(3*3)+(2*9)+(1*2)=92
92 % 10 = 2
So 4363-92-2 is a valid CAS Registry Number.

4363-92-2Relevant academic research and scientific papers

One-pot, three-step preparation of alkyl and aryl alkylcarbamates from S-methyl N-alkylthiocarbamates

Artuso, Emma,Degani, Iacopo,Fochi, Rita,Magistris, Claudio

experimental part, p. 1612 - 1618 (2009/04/03)

A general procedure for the synthesis of alkyl and aryl alkylcarbamates starting from the corresponding 5-methyl N-alkylthiocarbamates is described. This procedure consists of three steps that are carried out in a one-pot fashion, without isolating the intermediate N-alkylcarbamoyl chlorides or alkyl isocyanates. All the target products were obtained in high yields (16 examples, average yield 91%). To be noted is the recovery of a co-product of industrial interest, dimethyl disulfide, in a half mole amount for each mole of thiocarbamate, with complete exploitation of the reagent. The alkyl isocyanates, if required, can also be isolated in high yields. Georg Thieme Verlag Stuttgart.

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