(2S)-2-Phenyl-1-propanamine

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Names

[ CAS No. ]:
17596-79-1

[ Name ]:
(2S)-2-Phenyl-1-propanamine

[Synonym ]:
(S)-2-Phenylpropan-1-amine
(2S)-2-Phenyl-1-propanamine
Benzeneethanamine, β-methyl-, (βS)-
MFCD00216741
(2S)-2-phenylpropan-1-amine
(S)-(-)-2-Phenyl-1-propylamine
(S)-(-)-Beta-Methylphenethylamine
(S)-(-)-β-Methylphenethylamine

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
210.0±0.0 °C at 760 mmHg

[ Melting Point ]:
207 °C(lit.)

[ Molecular Formula ]:
C9H13N

[ Molecular Weight ]:
135.206

[ Flash Point ]:
79.4±0.0 °C

[ Exact Mass ]:
135.104797

[ PSA ]:
26.02000

[ LogP ]:
1.81

[ Vapour Pressure ]:
0.2±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.526

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 2735 8/PG 3

[ WGK Germany ]:
3

[ HS Code ]:
2921499090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 2-phenylpropylamine
  • 2-phenylpropionaldehyde
  • [(2R)-1-nitropropan-2-yl]benzene

DownStream

  • α-Cumyl alcohol
  • phenyl propanol
  • 2-Phenyl-1-propanol
  • (S)-1-PHENYLPROPAN-2-OL
  • (R)-1-Phenyl-2-propanol
  • Alpha,alpha-dimethylbenzyl chloride
  • 2-hydroxyethyl N-(2-phenylpropyl)carbamate

Customs

[ HS Code ]: 2921499090

[ Summary ]:
2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Structure–activity correlations for β-phenethylamines at human trace amine receptor 1

Bioorg. Med. Chem. 16 , 7415-23, (2008)

CoMFA 3D-QSAR studies on the potency of 68 β-phenethylamine analogs to activate hTAAR 1 (61% steric, 39% electrostatic) indicates that bulk both at nitrogen and 4-aryl leads to lower potency.

Kitagawa, M. Tatsuta, K.

Heterocycles 38 , 1747, (1994)


More Articles

Related Compounds

  • (2S)-2-Phenyl-1,4-butanediol
  • (2S)-2-Phenyl-1-butanol
  • (2S)-2-Phenyl-1,2,3,4-tetrahydroquinoline
  • (1R,2S)-(-)-2-phenyl-1-cyclopropane
  • (1R,2S)-2-phenyl-1-cyclohexyl (2R,3E)-2-hydroxy-3-octadecenoate
  • (1S,2S)-2-phenyl-1-(pyrrolidin-1-ylcarbonyl)cyclopropanecarboxylic acid
  • N-benzyl-N-ethyl-2-{[3-(4-methoxybenzyl)-4-oxo-3,4-dihydrothieno[3,2-d]pyrimidin-2-yl]sulfanyl}acetamide
  • N,N~2~-dicyclohexylglycinamide
  • 4-Chloro-6-(2-chloro-5-methoxyphenyl)pyrimidin-2-amine
  • 4-Chloro-6-(2,4-dichloro-5-methoxyphenyl)-2-pyrimidinamine
  • Diperodon anhydrous, (R)-
  • Dipipanone, (S)-
  • Guanidine, N-(((2R)-2,3-dihydro-1,4-benzodioxin-2-yl)methyl)-
  • Lactobionate
  • (Butan-2-yl)({[4-(trifluoromethoxy)phenyl]methyl})amine
  • (Butan-2-yl)[(2-nitrophenyl)methyl]amine
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