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2-[(2-OXO-2-P-TOLYL-ETHYL)-PHENYL-AMINO]-1-P-TOLYL-ETHANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

932022-92-9

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932022-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 932022-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,2,0,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 932022-92:
(8*9)+(7*3)+(6*2)+(5*0)+(4*2)+(3*2)+(2*9)+(1*2)=139
139 % 10 = 9
So 932022-92-9 is a valid CAS Registry Number.

932022-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-bis(4-methylphenacyl)aniline

1.2 Other means of identification

Product number -
Other names 2-[(2-oxo-2-p-tolyl-ethyl)-phenyl-amino]-1-p-tolyl-ethanone

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:932022-92-9 SDS

932022-92-9Relevant academic research and scientific papers

Ultrasound-mediated synthesis of N,N-bis(phenacyl)aniline under solvent-free conditions

He, Jingyu,Shi, Lanxiang,Liu, Sijie,Jia, Peng,Wang, Juan,Hu, Ruisheng

, p. 213 - 216 (2014/03/21)

An efficient method for the synthesis of N,N-bis(phenacyl)anilines was developed via smooth condensation of anilines with α-bromoacetophenones in the presence of sodium carbonate as acid acceptor and polyethylene glycol 400 (PEG 400) as catalyst at room t

Synthesis and photochemical properties of 2,4,6,-triaryl-4h-1,4-oxazines

Tan, Hongbo,Xin, Hongxing,Yan, Hong

, p. 359 - 373 (2014/03/21)

A series of 2,4,6-triaryl-4H-1,4-oxazines was synthesized, and their photochemical properties were studied. The 2,4,6-triaryl-4H-1,4-oxazines underwent photoreaction to N-(1-methoxy-2-oxo-2-arylethyl)-N-arylformamides determined by 1H NMR, 13C NMR, MS, and single crystal X-ray diffraction analyses.

Synthesis of 4H-1,4-oxazines as transthyretin amyloid fibril inhibitors

Li, Weipeng,Duan, Xiaowei,Yan, Hong,Xin, Hongxing

supporting information, p. 4546 - 4550 (2013/08/23)

4H-1,4-oxazines were designed as transthyretin (TTR) amyloid fibril inhibitors based on an analysis of the interactions between known small molecule inhibitors and TTR by molecular docking. A series of 2,4,6-triaryl-4H-1,4- oxazines was synthesized by the

Synthesis of novel 3,5,7-triaryl-5,6-dihydro-4H-1,2,5-triazepines

Ravindran, Gurusamy,Muthusubramanian, Shanmugam,Selvaraj, Sanguvan,Perumal, Subbu

, p. 133 - 136 (2008/09/16)

(Chemical Equation Presented) Several hitherto unknown 3,5,7-triaryl-5,6- dihydro-4H-1,2,5-triazepines have been synthesised by cyclocondensation of N,N-bis(phenacyl)anilines with hydrazine hydrate in ethanol or ethyleneglycol under reflux condition. Incr

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