ChemicalBook--->CAS DataBase List--->70138-19-1

70138-19-1

70138-19-1 Structure

70138-19-1 Structure
IdentificationBack Directory
[Name]

1-(3-METHYLPHENYL)ETHANAMINE
[CAS]

70138-19-1
[Synonyms]

1-(m-Tolyl)
1-(m-Tolyl)ethylamine
1-(M-tolyl)ethanaMine
3,α-Dimethylbenzylamine
1-(3-METHYLPHENYL)ETHANAMINE
1-(3-Methylphenyl)ethylamine
m-Methyl-alpha-phenethylamine
[1-(3-Methylphenyl)ethyl]amine
α,3-Dimethylbenzenemethanamine
m-Methyl-alpha-phenylethylamine
Benzenemethanamine, α,3-dimethyl-
BenzeneMethanaMine, a,3-diMethyl-
alpha,3-Dimethylbenzenemethanamine
BenzeneMethanaMine, .alpha.,3-diMethyl-
1-(3-methylphenyl)ethanamine(SALTDATA: FREE)
[Molecular Formula]

C9H13N
[MDL Number]

MFCD05215233
[MOL File]

70138-19-1.mol
[Molecular Weight]

135.21
Chemical PropertiesBack Directory
[Boiling point ]

204-205 °C
[density ]

0.9344 g/cm3
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

solid
[pka]

9.08±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
[InChI]

1S/C9H13N/c1-7-4-3-5-9(6-7)8(2)10/h3-6,8H,10H2,1-2H3
[InChIKey]

HIJMHAFOUAKOMS-UHFFFAOYSA-N
[SMILES]

CC(N)c1cccc(C)c1
Safety DataBack Directory
[Hazard Codes ]

Xi
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[HS Code ]

2921490090
[Storage Class]

11 - Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

1-(3-METHYLPHENYL)ETHANAMINE(70138-19-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

3'-Methylacetophenone

585-74-0

1-(3-METHYLPHENYL)ETHANAMINE

70138-19-1

General procedure for the synthesis of 1-(3-methylphenyl)ethylamine from 3'-methylacetophenone: an ethanol solution of 3'-methylacetophenone (400 mg, 2.13 mmol), Ti(Oi-Pr)4 (1.25 mL, 4.25 mmol) and ammonia (2M, 5.30 mL, 10.6 mmol) was stirred for 24 h at room temperature under argon protection. Subsequently, NaBH4 (120 mg, 3.19 mmol) was added and stirring was continued for 24 hours. Upon completion of the reaction, the pH of the reaction mixture was adjusted to 2 with 6 M HCl and washed with tert-butyl methyl ether (TBME) (3 x 20 mL). Next, the pH was adjusted to about 10 with NaOH (pelletized) and the mixture was extracted with TBME (6 x 30 mL). The organic phases were combined, dried over MgSO4 and the solvent was removed under reduced pressure to give 210 mg (1.11 mmol, 52%) of 1-(3-methylphenyl)ethylamine as a yellow oil.

[References]

[1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 12, p. 6002 - 6014
[2] Advanced Synthesis and Catalysis, 2016, vol. 358, # 3, p. 358 - 363
[3] Chirality, 2018, vol. 30, # 7, p. 900 - 906
[4] Bulletin des Societes Chimiques Belges, 1963, vol. 72, p. 202 - 207
[5] Collection of Czechoslovak Chemical Communications, 1973, vol. 38, p. 441 - 446
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