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N-TERT-BUTYLISOPROPYLAMINE

Basic Information

  • CAS No.: 7515-80-2
  • Purity: 99%
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Details

Factory Sells Best Quality N-TERT-BUTYLISOPROPYLAMINE 7515-80-2 with ISO standards

  • Molecular Formula: C7H17 N
  • Molecular Weight: 115.219
  • Vapor Pressure: 40.7mmHg at 25°C 
  • Melting Point: -38°C (estimate) 
  • Refractive Index: n20/D 1.398(lit.) 
  • Boiling Point: 98 °C(lit.)  
  • PKA: 10.76±0.38(Predicted) 
  • Flash Point: 26 °F  
  • PSA： 12.03000 
  • Density: 0.727 g/mL at 25 °C(lit.)  
  • LogP: 2.17380 

N-TERT-BUTYLISOPROPYLAMINE(Cas 7515-80-2) Usage

General Description

N-tert-Butylisopropylamine participates in the synthesis of hindered enamines.

InChI:InChI=1/C7H17N/c1-6(2)8-7(3,4)5/h6,8H,1-5H3/p+1

7515-80-2 Relevant articles

Semi-heterogeneous Dual Nickel/Photocatalysis using Carbon Nitrides: Esterification of Carboxylic Acids with Aryl Halides

Pieber, Bartholom?us,Malik, Jamal A.,Cavedon, Cristian,Gisbertz, Sebastian,Savateev, Aleksandr,Cruz, Daniel,Heil, Tobias,Zhang, Guigang,Seeberger, Peter H.

supporting information, p. 9575 - 9580 (2019/06/25)

Cross-coupling reactions mediated by dua...

Dynamic Ureas with Fast and pH-Independent Hydrolytic Kinetics

Cai, Kaimin,Ying, Hanze,Cheng, Jianjun

supporting information, p. 7345 - 7348 (2018/06/11)

Low cost, high performance hydrolysable ...

Steric Hindrance Underestimated: It is a Long, Long Way to Tri- tert-alkylamines

Banert, Klaus,Heck, Manuel,Ihle, Andreas,Kronawitt, Julia,Pester, Tom,Shoker, Tharallah

, p. 5138 - 5148 (2018/05/17)

Ten different processes (Methods A-J) we...

A mild, copper-catalysed amide deprotection strategy: Use of tert-butyl as a protecting group

Evans, Vikki,Mahon, Mary F.,Webster, Ruth L.

supporting information, p. 7593 - 7597 (2014/12/10)

Mild methods for the deprotection of org...

7515-80-2 Process route

<i>tert</i>-butylamine
75-64-9

tert -butylamine

isopropyl bromide
75-26-3

isopropyl bromide

N-isopropyl-N-tert-butylamine
7515-80-2

N-isopropyl-N-tert-butylamine

Conditions
Conditions Yield
With hexanedinitrile; tetra-(n-butyl)ammonium iodide; at 60 - 75 ℃;
89%
With hexanedinitrile; tetra-(n-butyl)ammonium iodide; at 90 ℃; for 72h; Inert atmosphere;
75%
With hexanedinitrile; tetra-(n-butyl)ammonium iodide; at 53 - 78 ℃; for 30h; Heating;
71%
With hexanedinitrile; tetra-(n-butyl)ammonium iodide; Reflux;
65%
methanol
67-56-1

methanol

1-tert-butyl-1-isopropyl-3-phenylurea
1202047-19-5

1-tert-butyl-1-isopropyl-3-phenylurea

N-isopropyl-N-tert-butylamine
7515-80-2

N-isopropyl-N-tert-butylamine

N-phenyl methyl carbamate
2603-10-3

N-phenyl methyl carbamate

Conditions
Conditions Yield
at 20 ℃; for 1h;
99%

7515-80-2 Upstream products

  • 2307-69-9
    2307-69-9

    toluene-4-sulfonic acid isopropyl ester

  • 51608-99-2
    51608-99-2

    N-2,6-Dimethylphenyl-N'-t-Bu,N'-isopropylharnstoff

  • 75-64-9
    75-64-9

    tert -butylamine

  • 67-64-1
    67-64-1

    acetone

7515-80-2 Downstream products

  • 85523-00-8
    85523-00-8

    N-isopropyl-N,2-dimethylpropan-2-amine

  • 106-42-3
    106-42-3

    para-xylene

  • 110426-48-7
    110426-48-7

    C7 H16 N(1-) *K(1+)

  • 4957-14-6
    4957-14-6

    4,4'-dimethyldiphenylmethane

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