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Formamide, N-cyclohexyl-N-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68172-49-6

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68172-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68172-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,7 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68172-49:
(7*6)+(6*8)+(5*1)+(4*7)+(3*2)+(2*4)+(1*9)=146
146 % 10 = 6
So 68172-49-6 is a valid CAS Registry Number.

68172-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexyl-N-ethylformamide

1.2 Other means of identification

Product number -
Other names ethylcyclohexylformamide

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:68172-49-6 SDS

68172-49-6Relevant academic research and scientific papers

Preparation of tetraalkylformamidinium salts and related species as precursors to stable carbenes

Alder, Roger W.,Blake, Michael E.,Bufali, Simone,Butts, Craig P.,Guy Orpen,Schuetz, Jan,Williams, Stuart J.

, p. 1586 - 1593 (2007/10/03)

The preparation of a range of tetraalkylformamidinium salts for use as precursors for the formation of stable diamino-and amino-carbenes was discussed. The preparation methods included nucleophilic addition to formamides followed by trapping with electrophiles such as triflic anhydride and various methods of formamide activation. Exchange reactions involving orthoesters, the transamination of amidinium salts and alkylation methods were other methods suitable for the synthesis.

Inhibition of human alcohol dehydrogenases by formamides

Schindler, John F.,Berst, Kristine B.,Plapp, Bryce V.

, p. 1696 - 1701 (2007/10/03)

Human alcohol dehydrogenase (HsADH) comprises class I (α, β, and γ), class II (π), and class IV (σ) enzymes. Selective inhibitors of the enzymes could be used to prevent the metabolism of alcohols that form toxic products. Formamides are unreactive analog

Process for the preparation of formamides

-

, (2008/06/13)

A process for the preparation of formamides by reacting a tertiary amine with carbon monoxide in the presence of a solvent, a catalytic quantity of a copper salt and oxygen or an oxygen-containing gaseous mixture. The reaction is preferably carried out in the presence of excess amine, a volatile alcohol solvent, and a copper halide catalyst.

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