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"Acetamide, N-(6-oxo-1-cyclohexen-1-yl)-" is a chemical compound with the molecular formula C9H11NO2. It is a derivative of acetamide, where the hydrogen atom on the nitrogen is replaced by a 6-oxo-1-cyclohexen-1-yl group. Acetamide, N-(6-oxo-1-cyclohexen-1-yl)- is characterized by a cyclohexene ring with a carbonyl group at the 6-position, which is connected to the nitrogen atom of the acetamide moiety. It is an organic compound that may be used in various chemical syntheses or as an intermediate in the production of pharmaceuticals or other organic compounds. The compound's structure provides it with unique chemical properties, making it a potentially valuable component in the development of new materials or drugs.

5908-28-1

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5908-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5908-28-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,0 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5908-28:
(6*5)+(5*9)+(4*0)+(3*8)+(2*2)+(1*8)=111
111 % 10 = 1
So 5908-28-1 is a valid CAS Registry Number.

5908-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(6-oxocyclohexen-1-yl)acetamide

1.2 Other means of identification

Product number -
Other names Acetamide,N-(6-oxo-1-cyclohexen-1-yl)

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 -
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More Details:5908-28-1 SDS

5908-28-1Relevant academic research and scientific papers

Decomposition of 2-Azido Ketones to 2-(Acetylamino)-2-alken-1-ones by Perrhenate Catalysis

Effenberger, Franz,Beisswenger, Thomas,Az, Rainer

, p. 4869 - 4876 (2007/10/02)

The thermally induced elimination of nitrogen from cyclic and acyclic 2-azido ketones 2 is accelerated by catalytic amounts of perrhenate.In acetic anhydride - if necessary in the presence of small amounts of a mineral acid - 2-(acetylamino)-2-alken-1-ones 3 are formed in good yields.The decomposition rates of the catalysed and the uncatalysed thermolysis are compared.

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