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4-[(4-chlorophenyl)imino]cyclohexa-2,5-dien-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68141-97-9

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68141-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68141-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,4 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68141-97:
(7*6)+(6*8)+(5*1)+(4*4)+(3*1)+(2*9)+(1*7)=139
139 % 10 = 9
So 68141-97-9 is a valid CAS Registry Number.

68141-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chlorophenyl)iminocyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,5-Cyclohexadien-1-one,4-((4-chlorophenyl)imino)

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:68141-97-9 SDS

68141-97-9Downstream Products

68141-97-9Relevant academic research and scientific papers

Palladium-catalyzed carbonylation of iminoquinones and aryl iodides to access arylp-amino benzoates

Wang, Siqi,Wu, Xiao-Feng,Yao, Lingyun,Ying, Jun

supporting information, p. 8246 - 8249 (2021/10/12)

A palladium-catalyzed carbonylation of iminoquinones and aryl iodides has been developed for the construction of arylp-amino benzoates. Using benzene-1,3,5-triyl triformate (TFBen) as the CO source, the reaction proceeded well to give various arylp-amino benzoates in good to excellent yields. Additionally, control experiments were conducted to gain more insights into the reaction mechanism.

OXIDATION OF AROMATIC AMINES WITH CHROMYL CHLORIDE - I OXYDATION OF AROMATIC PRIMARY AMINES

Nallaiah, C.,Strickson, J. A.

, p. 4083 - 4088 (2007/10/02)

The oxidation of aromatic primary amines with chromyl chloride in carbon tetrachloride or chloroform, results in the formation of intermediate solid adducts (Etard adducts) which, on hydrolysis, give azobenzenes(1), 1,4-benzoquinones(2), anilino-1,4-benzoquinones(3), 1,4-benzoquinone anils(4) and anilino-1,4-benzoquinone anils(5) in yields which depend on the position, nature and degree of substitution of the ring.

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