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2-(O-TOLYLAMINO)ETHANOL

  • CAS 136-80-1
  • Purity 99%
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Good factory supply good 2-(O-TOLYLAMINO)ETHANOL 136-80-1

  • Molecular Formula: C9H13 N O
  • Molecular Weight: 151.208
  • Vapor Pressure: 0.00131mmHg at 25°C 
  • Refractive Index: 1.5675 
  • Boiling Point: 285.5°C at 760 mmHg 
  • PKA: 14.68±0.10(Predicted) 
  • Flash Point: 145.6°C 
  • PSA： 32.26000 
  • Density: 1.086g/cm3 
  • LogP: 1.47220 

2-(O-TOLYLAMINO)ETHANOL(Cas 136-80-1) Usage

General Description

2-(o-Tolylamino)ethanol is a compound with the chemical formula C9H13NO that consists of a benzene ring attached to a hydroxyl group and an amino group. It is commonly used as a chemical intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. The compound has a molecular weight of 151.21 g/mol and a melting point of approximately 100-102°C. It is a colorless to light yellow liquid that is soluble in most organic solvents. 2-(o-Tolylamino)ethanol has potential applications in the pharmaceutical industry, as well as in research and development efforts for novel chemical compounds.

InChI:InChI=1/C9H13NO/c1-8-4-2-3-5-9(8)10-6-7-11/h2-5,10-11H,6-7H2,1H3

136-80-1 Relevant articles

Green synthesis of N-(2-hydroxyethyl)anilines by the selective alkylation reaction in H2O

Guo, Hui,Hao, Jia,Sun, Tingting,Wang, Zuoyao,Cao, Jian,Zhang, Guobao

, p. 1 - 6 (2020/07/21)

Based on our previous work, a safer and ...

β-Amino alcohols from anilines and ethylene glycol through heterogeneous Borrowing Hydrogen reaction

Llabres-Campaner, Pedro J.,Ballesteros-Garrido, Rafael,Ballesteros, Rafael,Abarca, Belén

supporting information, p. 5552 - 5561 (2017/08/22)

Borrowing Hydrogen (BH), also called Hyd...

A method for the preparation of indole compounds and use thereof (by machine translation)

-

Paragraph 0035-0039, (2018/04/01)

A method for the preparation of indole c...

Palladium-catalyzed intramolecular carbene insertion into C(sp3)-H bonds

Solé, Daniel,Mariani, Francesco,Bennasar, M.-Llu?sa,Fernández, Israel

supporting information, p. 6467 - 6470 (2016/06/01)

A palladium-catalyzed carbene insertion ...

136-80-1 Process route

ethylene glycol
107-21-1

ethylene glycol

<i>o</i>-toluidine
95-53-4

o -toluidine

7-methyl-1H-indole
933-67-5,261352-51-6

7-methyl-1H-indole

2-(2-tolylamino)ethan-1-ol
136-80-1

2-(2-tolylamino)ethan-1-ol

1,2-bis[(2-methylphenyl)amino]ethane
94-92-8

1,2-bis[(2-methylphenyl)amino]ethane

1,4-di-<i>o</i>-tolyl-piperazine
3367-47-3

1,4-di-o -tolyl-piperazine

Conditions
Conditions Yield
With palladium on activated charcoal; zinc(II) oxide; In water; at 150 ℃; for 24h; Sealed tube;
28%
20%
2-hydroxyethylchloramine
52316-60-6

2-hydroxyethylchloramine

toluene
108-88-3,15644-74-3,16713-13-6

toluene

1-(2-hydroxyethyl)amino-3-methylbenzene
102-41-0

1-(2-hydroxyethyl)amino-3-methylbenzene

2-[(4-methylphenyl)amino]-ethanol
2933-74-6

2-[(4-methylphenyl)amino]-ethanol

2-(2-tolylamino)ethan-1-ol
136-80-1

2-(2-tolylamino)ethan-1-ol

Conditions
Conditions Yield
With sulfuric acid; iron(II) sulfate; acetic acid; at 10 - 20 ℃; for 1.5h;
4%
11%
11%

136-80-1 Upstream products

  • 75-21-8
    75-21-8

    oxirane

  • 95-53-4
    95-53-4

    o -toluidine

  • 90869-76-4
    90869-76-4

    N-(o-tolyl)-(2-chloroethyl) carbamate

  • 107-07-3
    107-07-3

    2-chloro-ethanol

136-80-1 Downstream products

  • 3367-47-3
    3367-47-3

    1,4-di-o -tolyl-piperazine

  • 78182-25-9
    78182-25-9

    sulfuric acid mono-(2-o -toluidino-ethyl ester)

  • 28690-16-6
    28690-16-6

    phenyl-(3-o -tolyl-thiazolidin-2-yliden)-amine

  • 858844-90-3
    858844-90-3

    N '-benzoyl-N -(2-hydroxy-ethyl)-N -o -tolyl-thiourea

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