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6287-66-7

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6287-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6287-66-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6287-66:
(6*6)+(5*2)+(4*8)+(3*7)+(2*6)+(1*6)=117
117 % 10 = 7
So 6287-66-7 is a valid CAS Registry Number.

6287-66-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-oxo-4,6-diphenylcyclohex-3-ene-1-carboxylate

1.2 Other means of identification

Product number -
Other names 6-ethoxycarbonyl-3,5-diphenylcyclohex-2-en-1-one

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:6287-66-7 SDS

6287-66-7Relevant articles and documents

Base-promoted reactions in ionic liquid solvents. The Knoevenagel and Robinson annulation reactions

Morrison, Doug W,Forbes, David C,Davis Jr., James H

, p. 6053 - 6055 (2001)

When used in place of classical organic solvents, ionic liquids offer a new and environmentally benign approach toward solvation in modern synthetic chemistry. Two classical named reactions, the Knoevenagel condensation and Robinson annulation, have been

Nylon monomer and preparation method thereof

-

Paragraph 0028; 0031-0032, (2021/10/16)

The invention provides four nylon monomers and a preparation method thereof, wherein a nylon monomer is formed at 3 positions and 5 positions of a lactam or pimelic acid, and a preparation method of the nylon monomer is used for chalcone. The ethyl acetoa

Conversion of Simple Cyclohexanones into Catechols

Liang, Yu-Feng,Li, Xinyao,Wang, Xiaoyang,Zou, Miancheng,Tang, Conghui,Liang, Yujie,Song, Song,Jiao, Ning

supporting information, p. 12271 - 12277 (2016/09/28)

A novel I2-catalyzed direct conversion of cyclohexanones to substituted catechols under mild and simple conditions has been described. This novel transformation is remarkable with the multiple oxygenation and dehydrogenative aromatization processes enabled just by using DMSO as the solvent, oxidant, and oxygen source. This metal-free and simple system demonstrates a versatile protocol for the synthesis of highly valuable substituted catechols and therefore streamlines the synthesis and modification of biologically important molecules for drug discovery.

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