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37003-81-9

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37003-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37003-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,0 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 37003-81:
(7*3)+(6*7)+(5*0)+(4*0)+(3*3)+(2*8)+(1*1)=89
89 % 10 = 9
So 37003-81-9 is a valid CAS Registry Number.

37003-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methylanilino)-1-phenylbut-2-en-1-one

1.2 Other means of identification

Product number -
Other names (Z)-1-phenyl-3-(4-toluidino)-2-buten-1-one

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:37003-81-9 SDS

37003-81-9Downstream Products

37003-81-9Relevant articles and documents

Synthesis, characterization and crystal structure of (2Z)-3-[(4- methylphenyl)amino]-1-phenylbut-2-en-1-one

Patil, Siddappa A.,Gonzalez-Flores, Diego,Medina, Phillip A.,Vohs, Jason K.,Dever, Seth,Popp, Joshua,Stentzel, Michael,Pineda, Leslie W.,Montero, Mavis L.,Fahlman, Bradley D.

, p. 560 - 565 (2012)

The compound (2Z)-3-[(4-methylphenyl)amino]- 1-phenylbut-2-en-1-one was synthesized by the condensation reaction of benzoylacetone with p-methylaniline and structurally characterized by 1H NMR, 13C NMR, IR, mass spectrometry, element

Nano-SiO2 catalyzed synthesis of β-enaminones under solvent free conditions

Alinezhad, Heshmatollah,Tajbakhsh, Mahmood,Sarkati, Malihe Norouzi,Zare, Mahboobe

, p. 1591 - 1596 (2016/08/16)

Nano-SiO2 efficiently catalyzed the synthesis of β-enaminones using direct condensation of various (cyclic and acyclic) β-diketones with aromatic and aliphatic amines under solvent-free conditions. This eco-friendly catalyst can be recovered and reused without significant loss of activity. This methodology provides a simple synthetic route to enaminones in excellent yields at room temperature. Graphical abstract: [Figure not available: see fulltext.]

Zinc triflate catalysed synthesis of β-enamino ketones(esters) under solvent-free conditions

Feng, Chengliang,Zhang, Shuguang,Cai, Jin,Chen, Junqing,Hu, Huayou,Ji, Min

, p. 626 - 629 (2013/11/06)

An efficient and mild procedure is described for the synthesis of a series of β-enamino ketones(esters) from 1,3-dicarbonyl compounds and aliphatic and aromatic amines using zinc triflate as the catalyst.

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