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

41120-12-1

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41120-12-1 Usage

Molecular structure

Consists of a phenyl-amino group, a 2-oxo-2-phenyl-ethyl group, and a 1-phenyl-ethanone group.

Type of compound

Ketone, as it contains a carbonyl group (C=O) bonded to two alkyl or aryl groups.

Amine group (-NH2)

The phenyl-amino group indicates the presence of an amine functional group.

Ketone group (C=O)

The 2-oxo-2-phenyl-ethyl group contains a carbonyl group, classifying the compound as a ketone.

Biological activity potential

The presence of both an amine and a ketone suggests that the compound may have biological activity, as these functional groups are commonly found in bioactive molecules.

Specific properties and uses

It is difficult to determine the specific properties and potential uses of 2-[(2-OXO-2-PHENYL-ETHYL)-PHENYL-AMINO]-1-PHENYL-ETHANONE without further information.

Check Digit Verification of cas no

The CAS Registry Mumber 41120-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,2 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41120-12:
(7*4)+(6*1)+(5*1)+(4*2)+(3*0)+(2*1)+(1*2)=51
51 % 10 = 1
So 41120-12-1 is a valid CAS Registry Number.

41120-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-oxo-2-phenylethyl)anilino]-1-phenyl-1-ethanone

1.2 Other means of identification

Product number -
Other names diphenacylaniline

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:41120-12-1 SDS

41120-12-1Relevant academic research and scientific papers

A simple and efficient one-step synthesis of 2,4,10a-triaryl-1,10a-dihydro- 2H-pyrazino[2,1-b][1,3] benzothiazoles catalyzed by p-toluene sulfonic acid

Ravindran,Muthusubramanian,Selvaraj,Perumal

, p. 509 - 515 (2007)

A series of 2,4,10a-triaryl-1,10a-dihydro-2H-pyrazino[2,1-b][1,3] benzothiazoles were prepared in good yields by the reaction of 2-[(2-oxo-2-arylethyl) anilino]-1-aryl-1-ethanones with 2-aminothiophenol in the presence of p-toluenesulfonic acid under solv

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 oxathiane and morpholine from acyclic precursors: A modified Mitsunobu reaction

Paul, Nidhin,Kaladevi, Selvam,Beneto, Arockiam Jesin,Muthusubramanian, Shanmugam,Bhuvanesh, Nattamai

scheme or table, p. 6892 - 6901 (2012/09/11)

Synthesis of a set of isomeric 2,4,6-triarylmorpholines and 2,6-diaryloxathianes from the corresponding 1,5-diols has been described. The method provides an efficient route to six-membered heterocycles from acyclic diols and is found to be better than Mitsunobu procedure in yield and waste management. In a related study, the ring contraction of pyranone to two isomeric cyclopentenone derivatives through Nazarov reaction has been noticed.

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

A new approach to the preparation of 1,3,4-triarylpyrroles

De Zeng, Xing,Chen, Yi

, p. 490 - 492 (2007/10/03)

A class of 1,3,4-triaryl-2,5-dihydropyrroles were synthesized using the McMurry coupling reaction as the key step. The non-catalytic photoconversion of 1,3,4-triaryl-2,5-dihydropyrroles furnished 1,3,4-triarylpyrroles in good yields (63-89%). It was found

Study on photochromism of diarylethenes with a 2,5-dihydropyrrole bridging unit: A convenient preparation of 3,4-diarylpyrroles from 3,4-diaryl-2,5- dihydropyrroles

Chen, Yi,Zeng, De X.,Xie, Nan,Dang, Yi Z.

, p. 5001 - 5005 (2007/10/03)

Symmetric and nonsymmetric diarylethenes with a 2,5-dihydropyrrole bridging unit have been prepared, and the photochromic properties are investigated. Both symmetric and nonsymmetric diarylethenes with 2,5-dihydropyrrole bridging units undergo reversible ring-opening and ring-closing photoisomerization reactions in nonpolar solvents with UV/vis light, and some of them exhibit good fatigue resistance and no marked degradation detected after 10 cycles via an on/off switch. In polar solvents, however, photochromic diarylethenes with 2,5-dihydropyrrole bridging units produce 3,4-diarylpyrrole derivatives instead of the ring-closing isomer of diarylethenes with UV light irradiation. A class of N-substituted 3,4-diphenylethenes with 2,5-dihydropyrrole bridging units were prepared and used as templates to investigate the conversion reactions. The mechanism of photoconversion of 3,4-diaryl-2,5-dihydropyrroles to 3,4-diarylpyrroles was explored as well.

Photochemistry of N-heterocycles. 7: Light induced reductive ring contractions of sixmembered cyclic iminium ions

Nagy, Jozsef,Madarasz, Zoltan,Rapp, Rudolf,Szoelloesy, Aron,Nyitrai, Jozsef,Doepp, Dietrich

, p. 281 - 290 (2007/10/03)

Photochemically induced reductive ring contractions, previously observed for 2,5-dihydro-1,2,4-triazines, have also been verified for 1,4-dihydropyrimidines 2a,b, the dihydro-1,2,4,5-tetrazine 9, and dihydro-1,3,5-triazines 11a,b giving rise to fivemembered fully unsaturated heterocycles (pyrroles 4a,b, imidazoles 13a,b, and triazole 10, respectively). The 1,4-dihydropyrazines 15a-j tend to decompose in acidified 2-propanol in the dark, but on irradiation they also undergo reductive ring contraction furnishing solely the 1,2,5-triarylpyrroles 16a-d rather than the (a priori also possible) isomeric 1,3,4-triarylpyrroles 17a-d. In contrast, the 3,6-diphenylpyrid-azine 18 gives the 4-isopropyl-analogue 19 in low yield upon irradiation in hydrogen chloride saturated 2-propanol. Wiley-VCH Verlag GmbH, 2000.

Beckmann fragmentation of diphenylcarbamoylated N-aryldiphenacylamine dioximes. New method for the synthesis of imidazooxadiazolones

Coskun, Necdet,Tat, Fatma Tirli,Gueven, Oezden Oezel

, p. 3889 - 3894 (2007/10/03)

N-Aryl-N,N-diphenacylamine dioximes were prepared by the reaction of corresponding arylamines with α-bromoacetophenone oxime in ethanol-water at room temperature. These compounds reacted with aryl isocyanates in acetonitrile to give imidazooxadiazolones 9. The probable mechanism of the reaction is discussed.

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