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2-Cyclohexen-1-one, 2-[(4-nitrobenzoyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66049-46-5

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66049-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66049-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,4 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66049-46:
(7*6)+(6*6)+(5*0)+(4*4)+(3*9)+(2*4)+(1*6)=135
135 % 10 = 5
So 66049-46-5 is a valid CAS Registry Number.

66049-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(p-nitrobenzoyloxy)-2-cyclohexen-1-one

1.2 Other means of identification

Product number -
Other names 6-oxocyclohex-1-enyl 4-nitrobenzoate

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:66049-46-5 SDS

66049-46-5Relevant academic research and scientific papers

Preparation of N-arylamines from 2-oxo-7-azobicyclo[4.1.0]heptanes

Barros, M. Teresa,Dey, Suvendu S.,Maycock, Christopher D.,Rodrigues, Paula

supporting information; scheme or table, p. 6263 - 6268 (2012/08/28)

A wide range of N-phenylated secondary amines were prepared directly from 2-oxo-7-azobicyclo[4.1.0]heptanes using 4-nitrobenzoic acid as acid catalyst. The intermediate enol esters could also be isolated under similar conditions. A catalytic cycle is proposed.

Selectivity in 1,3-Dipolar cycloadditions of β-substituted captodative olefins - An experimental and DFT transition state study

Herrera, Rafael,Mendoza, Jorge A.,Morales, Miguel A.,Mendez, Francisco,Jimenez-Vazquez, Hugo A.,Delgado, Francisco,Tamariz, Joaquin

, p. 2352 - 2364 (2008/02/08)

Captodative olefins 1-acetylvinyl carboxylates substituted with alkyl groups at the β position, 12, strongly modified the regioselectivity of 1,3-dipolar cycloadditions with respect to the behavior observed for their unsubstituted analogs, 1. When the rea

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