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2-Phenylpropan-2-amine

Detailed Information

  • Product Name:2-Phenylpropan-2-amine
  • CasNo.:585-32-0
  • MF:C9H13N
  • MW:135.209

pd_nature

  • Purity:99%
  • pd_boiling:116°C (estimate)
  • Packing:Liquid. (Clear, colorless ~ yellow.)
  • Throughput:

Product Details;

CasNo: 585-32-0

MF: C9H13N

Appearance: Liquid. (Clear, colorless ~ yellow.)

Factory supply 2-Phenylpropan-2-amine 585-32-0 with sufficient stock and high standard

  • Molecular Formula:C9H13N
  • Molecular Weight:135.209
  • Appearance/Colour:Liquid. (Clear, colorless ~ yellow.) 
  • Melting Point:116°C (estimate) 
  • Refractive Index:1.5200 
  • Boiling Point:196.499 °C at 760 mmHg 
  • PKA:9.36±0.10(Predicted) 
  • Flash Point:84.05 °C 
  • PSA:26.02000 
  • Density:0.944 g/cm3 
  • LogP:2.58070 

CUMYLAMINE(Cas 585-32-0) Usage

Chemical Description

Cumylamine is an organic compound with the formula C9H13N.

InChI:InChI=1/C9H13N/c1-9(2,10)8-6-4-3-5-7-8/h3-7H,10H2,1-2H3

585-32-0 Relevant articles

Cerium-Catalyzed C-H Functionalizations of Alkanes Utilizing Alcohols as Hydrogen Atom Transfer Agents

An, Qing,Chen, Yuegang,Liu, Weimin,Pan, Hui,Wang, Xin,Wang, Ziyu,Zhang, Kaining,Zuo, Zhiwei

, p. 6216 - 6226 (2020/04/27)

Modern photoredox catalysis has traditio...

Carbon Dioxide-Mediated C(sp2)-H Arylation of Primary and Secondary Benzylamines

Kapoor, Mohit,Chand-Thakuri, Pratibha,Young, Michael C.

supporting information, p. 7980 - 7989 (2019/05/22)

C-C bond formation by transition metal-c...

Acid Is Key to the Radical-Trapping Antioxidant Activity of Nitroxides

Haidasz, Evan A.,Meng, Derek,Amorati, Riccardo,Baschieri, Andrea,Ingold, Keith U.,Valgimigli, Luca,Pratt, Derek A.

supporting information, p. 5290 - 5298 (2016/05/19)

Persistent dialkylnitroxides (e.g., 2,2,...

PRODUCTION METHOD FOR COMPOUND COMPRISING AMINO GROUP AND/OR HYDROXYL GROUP

-

Paragraph 0040; 0043, (2015/01/18)

Disclosed is a method for producing a co...

585-32-0 Process route

(1-methyl-1-phenyl-ethyl)-carbamic acid ethyl ester
1611-48-9

(1-methyl-1-phenyl-ethyl)-carbamic acid ethyl ester

ammonia
7664-41-7

ammonia

(1-methyl-1-phenyl-ethyl)-urea
58609-76-0

(1-methyl-1-phenyl-ethyl)-urea

urea
57-13-6

urea

urethane
51-79-6

urethane

2-phenyl-2-propylamine
585-32-0

2-phenyl-2-propylamine

Conditions
Conditions Yield
at 180 - 185 ℃;
cumyl azide
32366-26-0

cumyl azide

2-phenyl-2-propylamine
585-32-0

2-phenyl-2-propylamine

Conditions
Conditions Yield
With lithium aluminium tetrahydride; In diethyl ether; at 0 - 20 ℃; for 18h;
95%
With hydrogen; In ethanol; for 12h;
94%
With lithium aluminium tetrahydride; In diethyl ether; 1.) 12 h, 2.) reflux, 1 h;
68%
With Raney nickel; In isopropyl alcohol; at 60 - 70 ℃;
66%
With lithium aluminium tetrahydride; In diethyl ether; for 4h; Heating;
61.5%
With lithium aluminium tetrahydride; In diethyl ether; Heating;
nickel; In isopropyl alcohol;
With lithium aluminium tetrahydride; In diethyl ether; for 3h; Yield given; Ambient temperature;
With sodium chloride; nickel; In ethanol; Electrolysis;
With hydrogen; Lindlar's catalyst; In ethanol; for 12h;
19.8 g
With hydrogen; Lindlar's catalyst; In ethanol;
With palladium 10% on activated carbon; ammonium formate; In ethanol; at 50 ℃;
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
0.51 g

585-32-0 Upstream products

  • 826-54-0
    826-54-0

    2-methyl-2-phenyl-propanamide

  • 32366-26-0
    32366-26-0

    cumyl azide

  • 617-94-7
    617-94-7

    1-methyl-1-phenylethyl alcohol

  • 17797-08-9
    17797-08-9

    p-(2-Aminoprop-2-yl)-isopropylbenzol

585-32-0 Downstream products

  • 1611-48-9
    1611-48-9

    (1-methyl-1-phenyl-ethyl)-carbamic acid ethyl ester

  • 79649-68-6
    79649-68-6

    N-(1-methyl-1phenylethyl)acetamide

  • 66898-03-1
    66898-03-1

    N-(α,α-dimethylbenzyl)-p-toluenesulfonamide

  • 938-04-5
    938-04-5

    [1-(dimethylamino)-1-methylethyl]benzene

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