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2,5-Cyclohexadiene-1-carboxamide,1-(2-propenyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

245672-31-5

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245672-31-5 Usage

General Description

2,5-Cyclohexadiene-1-carboxamide, 1-(2-propenyl)-(9CI) is a chemical compound with the molecular formula C10H13NO. It is classified as an amide and contains a cyclohexadiene ring with a propenyl group attached to the carboxamide functional group. 2,5-Cyclohexadiene-1-carboxamide,1-(2-propenyl)-(9CI) has potential applications in the field of pharmaceuticals, as it may exhibit biological activity due to its structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 245672-31-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,6,7 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 245672-31:
(8*2)+(7*4)+(6*5)+(5*6)+(4*7)+(3*2)+(2*3)+(1*1)=145
145 % 10 = 5
So 245672-31-5 is a valid CAS Registry Number.

245672-31-5SDS

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 1-allyl-2,5-cyclohexadiene-1-carboxamide

1.2 Other means of identification

Product number -
Other names 1-Allyl-cyclohexa-2,5-dienecarboxylic acid amide

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:245672-31-5 SDS

245672-31-5Relevant academic research and scientific papers

Intramolecular conjugate addition reactions of amines and carbamates to 2,5-cyclohexadien-1-ones: Stereoselective synthesis of perhydroindoles

Bland, Douglas,Chambournier, Gilles,Dragan, Vladimir,Hart, David J.

, p. 8953 - 8966 (2007/10/03)

Intramolecular conjugate addition reactions of 4,4-disubstituted-2,5- cyclohexadien-1-ones are described within the context of possible approaches to manzamine A. Amine 4 provided tricycle 6, with improper relative stereochemistry for use in an approach to manzamine A. Carbamates 25 and 38 gave perhydroindoles 26 and 28 b under conditions of thermodynamic control, respectively, with the proper relative stereochemistry required for manzamine A. Carbamate 25 gave diastereomeric perhydroindole 27 under conditions of thermodynamic control.

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