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2-(2,5-Dimethyl-phenyl)-1,2-dihydro-quinoline is a chemical compound with the molecular formula C17H17N. It is a derivative of quinoline, a heterocyclic organic compound with a benzene ring fused to a pyridine ring. The compound features a 2,5-dimethylphenyl group attached to the quinoline core, which consists of two methyl groups at the 2nd and 5th positions of the phenyl ring. This structure endows the compound with unique chemical and physical properties, making it potentially useful in various applications, such as pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The compound's specific properties, reactivity, and applications depend on its molecular structure and the presence of the substituents.

76890-20-5

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76890-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76890-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,9 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76890-20:
(7*7)+(6*6)+(5*8)+(4*9)+(3*0)+(2*2)+(1*0)=165
165 % 10 = 5
So 76890-20-5 is a valid CAS Registry Number.

76890-20-5SDS

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 2-(2,5-dimethylphenyl)-1,2-dihydroquinoline

1.2 Other means of identification

Product number -
Other names -

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

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More Details:76890-20-5 SDS

76890-20-5Downstream Products

76890-20-5Relevant academic research and scientific papers

SYNTHESIS OF METHYL-SUBSTITUTED INDENOQUINOLINES, INDENOQUINOXALINES, AND THEIR KETO DERIVATIVES AND INVESTIGATION OF THEIR STRUCTURES

Prostakov, N. S.,Pleshakov, V. G.,Abedin, Md. Zainul,Kordova, I. R.,Zakharov, V. F.,Zvolinskii, V. P.

, p. 556 - 566 (2007/10/02)

A series of difficultly obtainable and previously unknown methyl homologs of 11H-indenoquinoline, 11H-indenoquinoxaline, and the corresponding 11-keto derivatives were synthesized by new convenient methods, and their structures were investigated.By PMR with lanthanide shift reagents Eu(dpm)3, Pr(dpm)3 and Yb(dpm)3 it was established that the indenoquinolines and ketoindenoquinoxalines do not coordinate with any of the indicated reagents, while the 11-keto derivatives of the indenoquinolines, like those of the indenoquinoxalines, only enter coordination with Yb(dpm)3 at the oxygen atom in the case of the ketoindenoqui nolines and at the N10 nitrogen atom in the case of the indenoquinoxalines.The results from quantum-chemical calculations on the keto derivatives of the indenoquinoline and indenoquinoxaline series are given, and the reasons for the various directions of coordination of Yb(dpm)3 with this type of compound are discussed.

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