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8-ETHYL-2-METHYLQUINOLINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72804-93-4

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72804-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72804-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,8,0 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72804-93:
(7*7)+(6*2)+(5*8)+(4*0)+(3*4)+(2*9)+(1*3)=134
134 % 10 = 4
So 72804-93-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N/c1-3-10-5-4-6-11-8-7-9(2)13-12(10)11/h4-8H,3H2,1-2H3

72804-93-4SDS

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 8-Ethyl-2-methylquinoline

1.2 Other means of identification

Product number -
Other names 8-Aethyl-2-methyl-chinolin

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:72804-93-4 SDS

72804-93-4Relevant academic research and scientific papers

Quinolines synthesis by reacting 1,3-butanediol with anilines in the presence of iron catalysts

Khusnutdinov,Bayguzina,Aminov

, p. 1613 - 1618 (2016/08/26)

2-, 4-, 6-, 7-, and 8-substituted quinolines were synthesized in 78–95% yield by the reaction of 1,3- butanediol with anilines in the presence of iron catalysts in carbon tetrachloride.

Synthesis of substituted quinolines by the reaction of anilines with alcohols and CCl4 in the presence of Fe-containing catalysts

Khusnutdinov,Bayguzina,Aminov

, p. 133 - 137 (2013/11/19)

Substituted quinolines were synthesized by the reaction of aniline derivatives with aliphatic alcohols and CCl4 upon the action of the FeCl3·6H2O catalyst.

TRIAZOLOPYRIDINE COMPOUNDS AS PIM KINASE INHIBITORS

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Page/Page column 93, (2012/12/13)

Compounds of Formula I: in which R1, R2, R3, R4 and R10 have the meanings given in the specification, are receptor tyrosine inhibitors useful in the treatment of diseases mediated by PIM-1 and/or PIM-2 and/or PIM-3 kinases.

Rhodium(I) Complexes of 8-Methyl-, 8-Ethyl-, and 8-Isopropyl-quinolines and Realated 2-Substituted Derivatives

Deeming, Antony J.,Rothwell, Ian P.

, p. 1259 - 1264 (2007/10/02)

The complexes have been prepared from on adding unidentate L (8-methyl-, -ethyl-, or -isopropyl-quinoline) or bidentate L (1,10-phenantroline or quinoline-2-carboxaldehide-N-methylimine). 8-Alkyl-substitution of the latter ligand gives the complexes as isomers with uni- and bi-dentate L respectively with relative stabilities of the unidentate form depending on the 8-substituent in the order Pri > Et > Me.Unidentate L is also favoured by replacing PPh3 by P(C6H11)3 but bidentate co-ordination is found using AsPh3 or PMe2Ph.Equilibrium constants for chloro-bridge cleavage of by 8-substituted and 2,8-disubstituted quinolines are reduced by increasing the size of the 8-susbtituent and even more by further introduction of a 2-methyl group.The contributions of distortions in the co-ordination to these changes in equilibrium constants are discussed.

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