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Carbamic acid, cyclohexylmethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56475-81-1

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56475-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56475-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,7 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56475-81:
(7*5)+(6*6)+(5*4)+(4*7)+(3*5)+(2*8)+(1*1)=151
151 % 10 = 1
So 56475-81-1 is a valid CAS Registry Number.

56475-81-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexyl,N-methylmethylcarbamate

1.2 Other means of identification

Product number -
Other names N-cyclohexyl-N-methyl carbamate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56475-81-1 SDS

56475-81-1Relevant academic research and scientific papers

Copper-Catalyzed Coupling of Amines with Carbazates: An Approach to Carbamates

Wang, Song-Ning,Zhang, Guo-Yu,Shoberu, Adedamola,Zou, Jian-Ping

, p. 9067 - 9075 (2021/07/19)

A new approach for the preparation of carbamatesviathe copper-catalyzed cross-coupling reaction of amines with alkoxycarbonyl radicals generated from carbazates is described. This environmentally friendly protocol takes place under mild conditions and is compatible with a wide range of amines, including aromatic/aliphatic and primary/secondary substrates.

Methoxycarbonylation of Alkyl-, Cycloalkyl-, and Arylamines with Dimethyl Carbonate in the Presence of Binder-Free Zeolite

Khazipova, A. N.,Khusnutdinov, R. I.,Mayakova, Yu. Yu.,Shchadneva, N. A.

, p. 1228 - 1235 (2020/10/02)

Abstract: Methyl N-alkyl-, N-cycloalkyl-, and N-arylcarbamates were synthesized by reaction of the correspondingamines with dimethyl carbonate in the presence of binder-free FeHY zeolite. Theoptimal conditions (reactant ratio, amount of the catalyst, temperature,reaction time) were found to afford the target products with high yields.

The syntheses of carbamates from reactions of primary and secondary aliphatic amines with dimethyl carbonate in ionic liquids

Sima, Tianlong,Guo, Shu,Shi, Feng,Deng, Youquan

, p. 8145 - 8147 (2007/10/03)

At 170°C and using ionic liquids as solvent and catalyst, primary and secondary aliphatic amines could react with dimethyl carbonate to give alkyl carbamates with good yield. Due to its insolubility, the desired carbamate solid could be recovered by simpl

Mechanistic Studies on the Role of Carbon Dioxide in the Synthesis of Methylcarbamates from Amines and Dimethylcarbonate in the Presence of CO2

Aresta, Michele,Quaranta, Eugenio

, p. 9489 - 9502 (2007/10/02)

N-Alkylmethylcarbamates have been synthesized from amines and dimethylcarbonate (DMC) in the presence of carbon dioxide.The catalytic role of CO2 in the overall process has been investigated and elucidated.Key words: carbon dioxide; organic carbamates; dimethylcarbonate; carbamic-carbonic anhydride

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