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N-(2-methylcyclohex-1-en-1-yl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56909-83-2

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56909-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56909-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,0 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56909-83:
(7*5)+(6*6)+(5*9)+(4*0)+(3*9)+(2*8)+(1*3)=162
162 % 10 = 2
So 56909-83-2 is a valid CAS Registry Number.

56909-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-methylcyclohex-1-en-1-yl)acetamide (en)Acetamide, N-(2-methyl-1-cyclohexen-1-yl)- (en)

1.2 Other means of identification

Product number -
Other names 1-Acetylamino-2-brom-5-chlor-benzol

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:56909-83-2 SDS

56909-83-2Relevant academic research and scientific papers

METHOD FOR PREPARING ENAMIDE COMPOUND AND RUTHENIUM COMPLEX CATALYST USED THEREIN

-

Paragraph 0114; 0115, (2017/10/27)

Provided is a method for preparing an enamide compound, which includes reacting an organic azide compound having α-hydrogen and an anhydride by addition of a ruthenium complex catalyst in the presence of an ionic liquid, and a ruthenium complex catalyst u

Synthesis of Enamides by Ruthenium-Catalyzed Reaction of Alkyl Azides with Acid Anhydrides in Ionic Liquid

Pak, Han Kyu,Han, Junghoon,Jeon, Mina,Kim, Yongjin,Kwon, Yearang,Park, Jin Yong,Rhee, Young Ho,Park, Jaiwook

, p. 4030 - 4034 (2015/12/26)

Enamides were synthesized by a ruthenium-catalyzed one-pot, one-step procedure from alkyl azides and acid anhydrides. The substrate scope includes not only secondary azides, but also primary aliphatic ones to give a wide range of enamides containing vario

An efficient synthesis of enamides from ketones

Hang, Zhao,Vandenbossche, Charles P.,Koenig, Stefan G.,Singh, Surendra P.,Bakale, Roger P.

, p. 505 - 507 (2008/09/19)

A new synthesis of enamides from ketones is disclosed that involves a phosphine-mediated reductive acylation of oximes. The resulting enamides are isolated in good yields (up to 89%) and excellent purity, permitting a subsequent hydrogenation to access en

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