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3-(DIMETHYLAMINO)-1-PHENYL-2-BUTEN-1-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34523-87-0

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34523-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34523-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,2 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34523-87:
(7*3)+(6*4)+(5*5)+(4*2)+(3*3)+(2*8)+(1*7)=110
110 % 10 = 0
So 34523-87-0 is a valid CAS Registry Number.

34523-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E)-3-(Dimethylamino)-1-phenyl-2-buten-1-one

1.2 Other means of identification

Product number -
Other names N,N'-Dimethyl-2-(2-(dimethylamino)ethyl)dithiomalonamide

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:34523-87-0 SDS

34523-87-0Relevant academic research and scientific papers

A simple synthesis of dimethyl 2-[(Z)-3-amino-1-oxo-1-(substituted)but-2-en-2-yl]fumarates: Potential intermediates in the synthesis of polysubstituted five- and six-membered heterocycles

?inkovec, Rok,Gro?elj, Uro?,Prek, Benjamin,Po?kaj, Marta,Ri?ko, Sebastijan,Svete, Jurij,Stanovnik, Branko

, p. 677 - 682 (2016/07/06)

In this communication, a simple synthesis of dimethyl 2-[(Z)-3-amino-1-oxo-1-(substituted)but-2-en-2-yl] fumarates is described. Methyl ketones were transformed by treatment with N,N-dimethylacetamide dimethyl acetal (DMADMA) into 3-dimethylamino-1-(subst

Reactions of methyl ketones and (hetero)arylcarboxamides with N,N-dimethylacetamide dimethyl acetal. A simple metal-free synthesis of 2,4,6-trisubstituted pyridines

Prek, Benjamin,Groelj, Uro,Kasuni, Marta,Zupani, Silvo,Svete, Jurij,Stanovnik, Branko

, p. 184 - 195 (2015/02/19)

Two metal-free syntheses of 2,4,6-trisubstituted pyridines 10a-m and 16a-j are described. N,N,6-Trimethyl-4-(substituted)pyridin-2-amines 10 were prepared from aryl or heteroaryl methyl ketones which were transformed with N,N-dimethylacetamide dimethyl ac

Clean and efficient synthesis of isoxazole derivatives in aqueous media

Dou, Guolan,Xu, Pan,Li, Qiang,Xi, Yukun,Huang, Zhibin,Shi, Daqing

, p. 13645 - 13653 (2014/01/06)

A series of 5-arylisoxazole derivatives were synthesized via the reaction of 3-(dimethyl-amino)-1-arylprop-2-en-1-ones with hydroxylamine hydrochloride in aqueous media without using any catalyst. This method has the advantages of easier work-up, mild rea

A SIMPLE PREPARATION OF SOME 4-METHYL-2H-PYRAN-2-ONES

Kepe, Vladimir,Polanc, Slovenko,Kocevar, Marijan

, p. 671 - 678 (2007/10/03)

A mehtod for the preparation of substituted 4-methyl-2H-pyran-2-ones (6-19) starting from methyl ketones (1), N,N-dimethylacetamide dimethyl acetal (2) and N-acylglycines (4) in acetic anhydride is described.

STUDY OF THE ESCHENMOSER SULFIDE CONTRACTION METHOD WITH AND WITHOUT A THIOPHILE

Corsaro, A.,Perrini, G.,Testa, M. G.,Chiacchio, U.

, p. 197 - 206 (2007/10/02)

Results obtained and observations made by applying the title method for the synthesis of enaminones 5a-o, using triphenylphosphine as a thiophile and triethylamine as a base, are reported.The product distributions of the deprotonations of α-phenacylthio iminium bromides with and without thiophile and those known from thiouronium and heterocyclic thionium analogs are compared.Key words: Enaminones; α-phenacylthio iminium bromides; disulfides; thiiranes.

A Simple Regioselective Synthesis of Pyrimidobenzimidazoles

Tseng, Shin-Shyong,Epstein, Joseph W.,Brabander, Herbert J.,Francisco, Gerardo

, p. 837 - 843 (2007/10/02)

2-Aminobenzimidazoles were reacted with enaminones in acetic acid to give pyrimidobenzimidazoles.With a substituted enaminone only one regioisomer was obtained.Structural assignments based on nmr and uv spectroscopy are presented.Possible pathways

Protonation and Acylation Reactions of Acyclic Enamino Ketones

Boehme, Horst,Traenka, Manfred

, p. 149 - 159 (2007/10/02)

α,β-Unsaturated β-dialkylamino ketones 4 are converted by means of tetrafluoroboric acid into thermodynamically stable Cα-protonated iminium salts 5. β-(Dialkylamino)vinyl ketones are shown to exist preferentially in the E-s-cis and E-s-trans c

New Synthesis of Isoxazoles and Isothiazoles. A Convenient Synthesis of Thioenaminones from Enaminones

Lin, Yang-i,Lang, Stanley, A.

, p. 4857 - 4860 (2007/10/02)

The reaction of 1-aryl-3-(dimethylamino)-2-propene-1-ones (enaminones) and 1-aryl-3-(dimethylamino)-2-propene-1-thiones (thioenaminones) with hydroxylamine-O-sulfonic acid gave, respectively, isoxazoles in 76-84 percent yields and isothiazoles in 60-65 pe

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