4-Methylphenethylamine

  • Name: 4-Methylphenethylamine
  • CAS: 3261-62-9
  • Purity: 99%
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Details

Top Quality Chinese Manufacturer supply 3261-62-9 4-Methylphenethylamine

  • Molecular Formula: C9H13N
  • Molecular Weight: 135.209
  • Appearance/Colour: clear colorless to light yellow liquid 
  • Vapor Pressure: 0.159mmHg at 25°C 
  • Melting Point: 116°C (estimate) 
  • Refractive Index: n20/D 1.527(lit.)  
  • Boiling Point: 214 °C at 760 mmHg 
  • PKA: 10.02±0.10(Predicted) 
  • Flash Point: 90.6 °C 
  • PSA： 26.02000 
  • Density: 0.95 g/cm3 
  • LogP: 2.19650 

4-Methylphenethylamine(Cas 3261-62-9) Usage

InChI:InChI=1/C9H13N/c1-8-2-4-9(5-3-8)6-7-10/h2-5H,6-7,10H2,1H3/p+1

3261-62-9 Relevant articles

Reduction of Aliphatic and Aromatic Nitro Compounds with Sodium Borohydride in Tetrahydrofuran Using 10percent Palladium-on-Carbon as Catalyst

Petrini, Marino,Ballini, Roberto,Rosini, Goffredo

, p. 713 - 714 (1987)

Aliphatic and aromatic nitro compounds a...

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Du, Yi-Dan,Chen, Bi-Hong,Shu, Wei

supporting information, p. 9875 - 9880 (2021/03/29)

Direct and selective synthesis of primar...

Benzimidazole fragment containing Mn-complex catalyzed hydrosilylation of ketones and nitriles

Ganguli, Kasturi,Mandal, Adarsha,Sarkar, Bidisha,Kundu, Sabuj

, (2020/08/13)

The synthesis of a new bidentate (NN)–Mn...

Bi-enzymatic Conversion of Cinnamic Acids to 2-Arylethylamines

Weise, Nicholas J.,Thapa, Prasansa,Ahmed, Syed T.,Heath, Rachel S.,Parmeggiani, Fabio,Turner, Nicholas J.,Flitsch, Sabine L.

, p. 995 - 998 (2020/01/21)

The conversion of carboxylic acids, such...

Combined Photoredox/Enzymatic C?H Benzylic Hydroxylations

Betori, Rick C.,May, Catherine M.,Scheidt, Karl A.

supporting information, p. 16490 - 16494 (2019/11/03)

Chemical transformations that install he...

3261-62-9 Process route

(4-methylphenyl)acetonitrile
2947-61-7

(4-methylphenyl)acetonitrile

2-(p-tolyl)ethylamine
3261-62-9

2-(p-tolyl)ethylamine

Conditions
Conditions Yield
With sodium tetrahydroborate; nickel; sodium hydroxide; In methanol; water; at 30 - 60 ℃;
92%
With lithium aluminium tetrahydride; diethyl ether;
With ethanol; sodium;
With ammonia; nickel; at 100 - 125 ℃; Hydrogenation;
With acetic anhydride; platinum; Hydrogenation.beim Erhitzen mit wss. HCl;
With sodium hydroxide; In water;
With [Ru(H2)H2(NC5H3(CH2P(C(CH3)3)2)2)]; water; hydrogen; In toluene; at 135 ℃; for 24h; under 56255.6 Torr; Autoclave;
95 %Chromat.
Multi-step reaction with 2 steps
1: C16 H11 BrMnN3 O3 / tetrahydrofuran / 24 h / 120 °C / Inert atmosphere; Sealed tube
2: sodium hydroxide; water / tetrahydrofuran; methanol / 20 °C
With water; C16H11BrMnN3O3; sodium hydroxide; In tetrahydrofuran; methanol;
C<sub>21</sub>H<sub>25</sub>NSi<sub>2</sub>

C21 H25 NSi2

2-(p-tolyl)ethylamine
3261-62-9

2-(p-tolyl)ethylamine

Conditions
Conditions Yield
With water; sodium hydroxide; In tetrahydrofuran; methanol; at 20 ℃;

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