ChemicalBook--->CAS DataBase List--->1026-05-7

1026-05-7

1026-05-7 Structure

1026-05-7 Structure
IdentificationBack Directory
[Name]

(2-METHYL-1,2,3,4-TETRAHYDRO-QUINOLIN-4-YL)-PHENYL-AMINE
[CAS]

1026-05-7
[Synonyms]

ASISCHEM N44996
AKOS BBS-00005674
2-Methyl-N-phenyl-1,2,3,4-tetrahydroquinolin-4-aMine
4-Quinolinamine, 1,2,3,4-tetrahydro-2-methyl-N-phenyl-
Quinaldine,4-anilino-1,2,3,4-tetrahydro- (6CI,7CI,8CI)
(2-METHYL-1,2,3,4-TETRAHYDRO-QUINOLIN-4-YL)-PHENYL-AMINE
N-(2-METHYL-1,2,3,4-TETRAHYDRO-4-QUINOLINYL)-N-PHENYLAMINE
Propanedinitrile,2-(3-cyano-4,5,5-trimethyl-2(7H)-furanylidene)-
[Molecular Formula]

C16H18N2
[MDL Number]

MFCD00183927
[MOL File]

1026-05-7.mol
[Molecular Weight]

238.33
Chemical PropertiesBack Directory
[Melting point ]

126 °C
[Boiling point ]

400.4±44.0 °C(Predicted)
[density ]

1.097±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

4.16±0.60(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

(2-METHYL-1,2,3,4-TETRAHYDRO-QUINOLIN-4-YL)-PHENYL-AMINE(1026-05-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-PHENYLAMINO-PROPIONIC ACID

15727-49-8

(2-METHYL-1,2,3,4-TETRAHYDRO-QUINOLIN-4-YL)-PHENYL-AMINE

1026-05-7

General procedure for the synthesis of 2-methyl-N-phenyl-1,2,3,4-tetrahydroquinolin-4-amine from 2-phenylaminopropionic acid: 2-phenylaminopropionic acid (66 mg, 0.4 mmol) and 4?molecular sieves (100 mg) were added to a 10 mL reaction vial, dried with an air pump, and then 200 μL of a reaction vial containing an organic photocatalyst, DPZ (0.28 mg 0.0008 mmol) in toluene solution. Subsequently, 4 mL of purified water was added, the reaction mixture was dried with chloroform, and the mouth of the flask was sealed with a rubber stopper and a balloon filled with dry air was inserted. The reaction flask was placed in a 25°C incubator and the reaction was stirred for 15 h under the illumination of two 1 W blue LEDs. Upon completion of the reaction, about 2/3 of the solvent was removed by distillation using a rotary evaporator. Purification by column chromatography (eluent: hexane/ethyl acetate, 60:30:1) afforded 2-methyl-N-phenyl-1,2,3,4-tetrahydroquinolin-4-amine (39.1 mg, 82% yield) as a colorless oily liquid.

[References]

[1] Patent: CN108017579, 2018, A. Location in patent: Paragraph 0008; 0011; 0012
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