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3,4-diphenylbut-3-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38661-88-0

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38661-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38661-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,6 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38661-88:
(7*3)+(6*8)+(5*6)+(4*6)+(3*1)+(2*8)+(1*8)=150
150 % 10 = 0
So 38661-88-0 is a valid CAS Registry Number.

38661-88-0SDS

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 (E)-3,4-diphenylbut-3-en-2-one

1.2 Other means of identification

Product number -
Other names 3,4t-Diphenyl-but-3-en-2-on

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:38661-88-0 SDS

38661-88-0Relevant academic research and scientific papers

Stereospecific Decarboxylative Nazarov Cyclization Mediated by Carbon Dioxide for the Preparation of Highly Substituted 2-Cyclopentenones

Komatsuki, Keiichi,Sadamitsu, Yuta,Sekine, Kohei,Saito, Kodai,Yamada, Tohru

, p. 11594 - 11598 (2017/09/11)

Highly substituted 2-cyclopentenones were stereospecifically and regioselectively constructed with high catalytic efficiency through Lewis-acid catalyzed decarboxylative Nazarov cyclization of the cyclic carbonate derivative, which is prepared by reacting the propargyl alcohol with carbon dioxide in the presence of a silver catalyst. The stereochemistry of the 2-cyclopentenone is strictly controlled by the geometry of the alkene in the starting material. This method is applicable for various substrates.

Acid-catalyzed synthesis of α,β-disubstituted conjugated enones by a Meyer-Schuster-type rearrangement in allenols

Alcaide, Benito,Almendros, Pedro,Cembellín, Sara,Martínez Del Campo, Teresa

, p. 1070 - 1078 (2015/03/30)

A novel, direct and simple methodology to gain access to α,β-disubstituted conjugated enones from α-allenols in a sustainable metal catalysis context, considering the inexpensiveness and environmentally friendliness of iron(III) species and protons, has b

Copper-catalyzed regio- and stereoselective intermolecular three-component oxyarylation of allenes

Itoh, Taisuke,Shimizu, Yohei,Kanai, Motomu

supporting information, p. 2736 - 2739 (2014/06/09)

A copper(II)-catalyzed intermolecular three-component oxyarylation of allenes using arylboronic acids as a carbon source and TEMPO as an oxygen source is described. The reaction proceeded under mild conditions with high regio- and stereoselectivity and functional group tolerance. A plausible reaction mechanism is proposed, involving carbocupration of allenes, homolysis of the intervening allylcopper(II), and a radical TEMPO trap.

Synthesis and antimicrobial evaluation of some pyrazole derivatives

Sharshira, Essam Mohamed,Hamada, Nagwa Mohamed Mahrous

scheme or table, p. 4962 - 4971 (2012/09/22)

Reaction of a series of (E)-3-phenyl-4-(p-substituted phenyl)-3-buten-2- ones with p-sulfamylphenyl hydrazine in glacial acetic acid gave the corresponding hydrazones, subsequent treatment of which with 30% HCl afforded pyrazole-1-sulphonamides. On the ot

Iridium-catalyzed asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones: Enantioselective total synthesis of (-)-mesembrine

Zhang, Qian-Qian,Xie, Jian-Hua,Yang, Xiao-Hui,Xie, Jian-Bo,Zhou, Qi-Lin

supporting information, p. 6158 - 6161 (2013/02/23)

A highly efficient asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones catalyzed by chiral spiro iridium complexes for the preparation of chiral 2-substituted allylic alcohols has been developed (ee up to 99.7%). This method provides a concise route to (-)-mesembrine (34% yield, 12 steps).

Palladium-catalyzed oxidative cross-coupling reaction of arylboronic acids with diazoesters for stereoselective synthesis of (E)-α,β- diarylacrylates

Tsoi, Yuk-Tai,Zhou, Zhongyuan,Chan, Albert S. C.,Yu, Wing-Yiu

supporting information; experimental part, p. 4506 - 4509 (2010/12/25)

A Pd-catalyzed oxidative cross-coupling reaction of arylboronic acids with α-diazoesters was achieved using molecular oxygen as the sole reoxidant, and E-α,β-diarylacrylates were obtained in good yields and >20:1 E-to-Z selectivity.

CuH-catalyzed enantioselective 1,2-reductions of α,β-unsaturated ketones

Moser, Ralph,Boskovia, Zarko V.,Crowe, Christopher S.,Lipshutz, Bruce H.

supporting information; experimental part, p. 7852 - 7853 (2010/08/04)

The first study on a general technology for arriving at valued nonracemic allylic alcohols using asymmetric ligand-accelerated catalysis by copper hydride is described.

A nonsymmetric pincer-catalyzed Suzuki-Miyaura arylation of benzyl halides and other nonactivated unusual coupling partners

Ines, Blanca,Moreno, Isabel,SanMartin, Raul,Dominguez, Esther

supporting information; experimental part, p. 8448 - 8451 (2009/04/11)

(Chemical Equation Presented) The catalytic activity of a PCN-type palladium pincer complex is evaluated in the construction of C(sp 2)-C(sp2) and C(sp2)-C(sp3) bonds by Suzuki-Miyaura cross-couplings employing nontypical substrates such as benzyl halides, α-haloenones, or alkylboronic acids as coupling partners. Most of the reported reactions are achieved in aqueous media, with all of the advantages implied.

Highly enantioselective synthesis of optically active ketones by iridium-catalyzed asymmetric hydrogenation

Lu, Sheng-Mei,Bolm, Carsten

supporting information; experimental part, p. 8920 - 8923 (2009/05/30)

(Chemical Equation Presented) Close to perfect enantioselectivity (up to 99% ee, see scheme) is found for the formation of α-substituted ketones by the asymmetric hydrogenation of enones with an iridium-phosphinooxazoline catalyst. In an operationally simple process, both linear and cyclic substrates react well and afford the desired products in high yields. A wide variety of substituents are tolerated, thus making the method synthetically appealing.

The α-arylation of α-bromo- and α-chloroenones using palladium-catalysed cross-coupling

Banks, James C.,Mele, David Van,Frost, Christopher G.

, p. 2863 - 2866 (2007/10/03)

The palladium-catalysed cross-coupling reaction of various arylboronic acids with α-bromoenones and α-chloroenones offers an operationally simple approach to the synthesis of both cyclic and acyclic α-arylenones.

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