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

96604-34-1

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96604-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96604-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,0 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96604-34:
(7*9)+(6*6)+(5*6)+(4*0)+(3*4)+(2*3)+(1*4)=151
151 % 10 = 1
So 96604-34-1 is a valid CAS Registry Number.

96604-34-1Relevant 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

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

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