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3,3-Diphenylpropanol

Basic Information

  • CAS No.: 20017-67-8
  • Purity: 99%
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Details

Factory sells 3,3-Diphenylpropanol 20017-67-8 with sufficient production capacity

  • Molecular Formula: C15H16O
  • Molecular Weight: 212.291
  • Vapor Pressure: 9.38E-05mmHg at 25°C 
  • Melting Point: 20-22 °C(Solv: heptane (142-82-5)) 
  • Refractive Index: n20/D 1.584(lit.)  
  • Boiling Point: 325.5 °C at 760 mmHg 
  • PKA: 14.97±0.10(Predicted) 
  • Flash Point: 149.1 °C 
  • PSA： 20.23000 
  • Density: 1.06 g/cm3 
  • LogP: 3.20090 

3,3-Diphenylpropanol(Cas 20017-67-8) Usage

Synthesis Reference(s)

Canadian Journal of Chemistry, 65, p. 2734, 1987 DOI: 10.1139/v87-455Synthetic Communications, 24, p. 591, 1994 DOI: 10.1080/00397919408012636

General Description

3,3-Diphenyl-1-propanol undergoes cobalt-catalyzed hydroformylation reaction to give the corresponding aldehyde and 1,1-diphenylethylene.

InChI:InChI=1/C15H16O/c16-12-11-15(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10,15-16H,11-12H2

20017-67-8 Relevant articles

Weinreb Amide as Secondary Station for the Dibenzo-24-crown-8 in a Molecular Shuttle

Gauthier, Maxime,Coutrot, Frédéric

, p. 3391 - 3395 (2019)

Here is reported the synthesis of a new ...

RHODIUM AND COBALT CATALYSIS OF THE HYDROFORMYLATION AND HYDROGENATION OF 1,1-DIPHENYLETHYLENE

Matsui, Yasushi,Orchin, Milton

, p. 57 - 60 (1983)

Rhodium and cobalt catalyzed reactions o...

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Hauser et al.

, p. 916 (1958)

-

-

Protiva

, (1951)

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Umpolung Strategy for Arene C?H Etherification Leading to Functionalized Chromanes Enabled by I(III) N-Ligated Hypervalent Iodine Reagents

Mikhael, Myriam,Guo, Wentao,Tantillo, Dean J.,Wengryniuk, Sarah E.

supporting information, p. 4867 - 4875 (2021/09/14)

The direct formation of aryl C?O bonds v...

Weinreb Amide, Ketone and Amine as Potential and Competitive Secondary Molecular Stations for Dibenzo-[24]Crown-8 in [2]Rotaxane Molecular Shuttles

Coutrot, Frédéric,Gauthier, Maxime

supporting information, p. 17576 - 17580 (2021/12/09)

This paper reports the synthesis and stu...

Exploring the synthetic potential of a marine transaminase including discrimination at a remote stereocentre

Schwarz, Maria,Murphy, Edel J.,Foley, Aoife M.,Woods, David F.,Castilla, Ignacio Abreu,Reen, F. Jerry,Collins, Stuart G.,O'gara, Fergal,Maguire, Anita R.

supporting information, p. 188 - 198 (2021/01/18)

The marine transaminase, P-ω-TA, can be ...

20017-67-8 Process route

3,3-diphenylprop-2-en-1-ol
4801-14-3

3,3-diphenylprop-2-en-1-ol

1,1-diphenylpropane
1530-03-6

1,1-diphenylpropane

3,3-diphenylpropan-1-ol
20017-67-8

3,3-diphenylpropan-1-ol

Conditions
Conditions Yield
With palladium 10% on activated carbon; hydrogen; In methanol; for 19h; under 3000.3 Torr;
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

3,3-diphenylpropyllithium
85316-26-3

3,3-diphenylpropyllithium

1,1,4,4-tetraphenyl-butane
1483-64-3

1,1,4,4-tetraphenyl-butane

Diphenylmethane
101-81-5

Diphenylmethane

1,1-diphenylpentane
1726-12-1

1,1-diphenylpentane

1,1-diphenylpropane
1530-03-6

1,1-diphenylpropane

3,3-diphenylpropan-1-ol
20017-67-8

3,3-diphenylpropan-1-ol

trimethylsilyldiphenylmethane
6328-61-6

trimethylsilyldiphenylmethane

Conditions
Conditions Yield
With bis-pentadeuterioethyl ether; Product distribution; Mechanism;
71.82 % Chromat.
15.10 % Chromat.
7.75 % Chromat.
1.33 % Chromat.
1.04 % Chromat.
0.16 % Chromat.

20017-67-8 Upstream products

  • 101-81-5
    101-81-5

    Diphenylmethane

  • 606-83-7
    606-83-7

    3,3-Diphenylpropionic acid

  • 7476-18-8
    7476-18-8

    3,3-diphenyl-propionic acid ethyl ester

  • 856817-59-9
    856817-59-9

    acetic acid-(3,3-diphenyl-propyl ester)

20017-67-8 Downstream products

  • 3540-95-2
    3540-95-2

    fenpiprane

  • 20017-68-9
    20017-68-9

    1-bromo-3,3-diphenylpropane

  • 71313-79-6
    71313-79-6

    C28 H22 Cl2 N2 O7

  • 530-48-3
    530-48-3

    1,1-Diphenylethylene

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