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3-Quinolinol, 1,2,3,4-tetrahydro-1-phenyl-, also known as 1-Phenyl-1,2,3,4-tetrahydroquinoline, is an organic compound with the chemical formula C15H15N. It is a derivative of quinoline, a heterocyclic aromatic compound consisting of a benzene ring fused to a pyridine ring. This particular compound features a phenyl group attached to the nitrogen atom and a saturated ring structure, making it a tetrahydroquinoline. It is a colorless to pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its unique structure and properties, 1-Phenyl-1,2,3,4-tetrahydroquinoline has potential applications in the development of new drugs and materials.

3297-75-4

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3297-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3297-75-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3297-75:
(6*3)+(5*2)+(4*9)+(3*7)+(2*7)+(1*5)=104
104 % 10 = 4
So 3297-75-4 is a valid CAS Registry Number.

3297-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3,4-dihydro-2H-quinolin-3-ol

1.2 Other means of identification

Product number -
Other names 1-Phenyl-1,2,3,4-tetrahydro-chinolin-3-ol

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:3297-75-4 SDS

3297-75-4Relevant academic research and scientific papers

Titanocene(III)-catalyzed conversion of N-(epoxyalkyl)anilines into indolines

MacIejewski, John P.,Wipf, Peter

, p. 92 - 119 (2011/06/20)

Densely substituted indolines and azaindolines can be obtained by the titanocene(III) chloride catalyzed reductive opening of N-(oxiran-2-ylmethyl) anilines. The reaction optimization, substrate scope, and limitations are discussed, and a mechanistic pathway for the epoxideopening rearrangement is proposed. ARKAT-USA, Inc.

Copper(II)-catalyzed aminooxygenation and carboamination of N-aryl-2-allylanilines

Sherman, Eric S.,Chemler, Sherry R.

supporting information; experimental part, p. 467 - 471 (2009/11/30)

The scope of the intramolecular copper(II)-catalyzed carboamination and aminooxygenation reactions of olefins has been extended to include N-aryl-2-allylanilines. These substrates exhibit divergent reactivity under catalytic vs. stoichiometric conditions.

Titanocene(III)-catalyzed formation of indolines and azaindolines

Wipf, Peter,Maciejewski, John P.

supporting information; experimental part, p. 4383 - 4386 (2009/05/30)

(Chemical Equation Presented) Reductive cyclization of epoxides tethered to substituted anilines and aminopyridines in the presence of 3 mol % of titanocene dichloride and stoichiometric manganese metal promotes a radical annulation to form 3,3-disubstituted indolines and azaindolines.

Synthesis and thermal reactions of N-(2,3-epoxypropyl)diphenylamine

Barvainiene,Stanisauskaite,Getautis

, p. 718 - 721 (2008/03/11)

The synthesis of N-(2,3-epoxypropyl)diphenylamine is reported. It was found that thermal opening of the oxirane ring of N-(2,3-epoxypropyl)diphenylamine occurred both at the secondary and the tertiary carbon atoms but the basic reaction product is 3-hydro

Hydrazones possessing a phenyl-1,2,3,4-tetrahydroquinoline moiety as hole transporting materials

Getautis, Vytautas,Stanisauskaite, Albina,Malinauskas, Tadas,Stumbraite, Jolanta,Gaidelis, Valentas,Jankauskas, Vygintas

, p. 1401 - 1409 (2007/10/03)

Hydrazones containing 1-phenyl-1,2,3,4-tetrahydroquinoline units were synthesized starting from diphenylamine. These compounds were found to constitute novel hole transporting materials and were characterized by the time of flight method. The hole drift m

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