2,3-diphenylpropanol

  • Name: 2,3-diphenylpropanol
  • CAS: 3536-29-6
  • Purity: 99%
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Details

2,3-diphenylpropanol Good Manufacturer supply High Quality 3536-29-6

  • Molecular Formula: C15H16 O
  • Molecular Weight: 212.291
  • Vapor Pressure: 6.41E-05mmHg at 25°C 
  • Melting Point: 51°C 
  • Refractive Index: 1.5742 (estimate) 
  • Boiling Point: 331°Cat760mmHg 
  • Flash Point: 134.4°C 
  • PSA： 20.23000 
  • Density: 1.073g/cm3 
  • LogP: 3.00520 

2,3-diphenylpropanol(Cas 3536-29-6) Usage

General Description

2,3-diphenylpropanol, also known as 2,3-diphenyl-1-propanol, is a chemical compound with the formula C15H16O. It is a white, crystalline solid with a mild floral odor. It is commonly used as a fragrance and flavor ingredient in various products. It is also used as a chiral auxiliary in organic synthesis and as a starting material for the synthesis of other compounds. Additionally, 2,3-diphenylpropanol has been studied for its potential biological activities, including its anti-inflammatory and antioxidant properties. However, further research is needed to fully understand its potential uses and effects.

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

3536-29-6 Relevant articles

Highly efficient NHC-iridium-catalyzed β-methylation of alcohols with methanol at low catalyst loadings

Lu, Zeye,Zheng, Qingshu,Zeng, Guangkuo,Kuang, Yunyan,Clark, James H.,Tu, Tao

, p. 1361 - 1366 (2021/06/30)

The methylation of alcohols is of great ...

Cross β-alkylation of primary alcohols catalysed by DMF-stabilized iridium nanoparticles

Kobayashi, Masaki,Yamaguchi, Hiroki,Suzuki, Takeyuki,Obora, Yasushi

supporting information, p. 1950 - 1954 (2021/03/16)

A simple method for the cross β-alkylati...

Cross β-arylmethylation of alcohols catalysed by recyclable Ti-Pd alloys not requiring pre-activation

Utsunomiya, Masayoshi,Kondo, Ryota,Oshima, Toshinori,Safumi, Masatoshi,Suzuki, Takeyuki,Obora, Yasushi

supporting information, p. 5139 - 5142 (2021/05/31)

Ti-Pd alloy catalysts were developed for...

syn-Selective Michael Reaction of α-Branched Aryl Acetaldehydes with Nitroolefins Promoted by Squaric Amino Acid Derived Bifunctional Br?nsted Bases

Campano, Teresa E.,García-Urricelqui, Ane,Mielgo, Antonia,Palomo, Claudio,de Cózar, Abel

supporting information, p. 3604 - 3612 (2021/07/26)

Here we describe a direct access to 2,2,...

3536-29-6 Process route

2,3-diphenylpropanal
2016-03-7

2,3-diphenylpropanal

1,2-diphenylpropene
833-81-8,1017-22-7,34473-62-6,85165-70-4,779-51-1

1,2-diphenylpropene

1,3-diphenylpropene
3412-44-0,1138-83-6,5209-18-7

1,3-diphenylpropene

1,2-diphenylpropane
5814-85-7

1,2-diphenylpropane

1,3-diphenylpropane
1081-75-0

1,3-diphenylpropane

2,3-diphenyl-1-propanol
3536-29-6

2,3-diphenyl-1-propanol

Conditions
Conditions Yield
With mercury; zinc; In hydrogenchloride; for 2h; Product distribution; Heating;
2 % Chromat.
35 % Chromat.
9 % Chromat.
14 % Chromat.
40 % Chromat.
ethanol
64-17-5

ethanol

ethyl 2,3-diphenylacrylate
24446-63-7

ethyl 2,3-diphenylacrylate

1,2-diphenylpropane
5814-85-7

1,2-diphenylpropane

2,3-diphenyl-1-propanol
3536-29-6

2,3-diphenyl-1-propanol

2,3-diphenylpropanoic acid
94942-89-9

2,3-diphenylpropanoic acid

Conditions
Conditions Yield
trans-form;

3536-29-6 Upstream products

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    22379-62-0

    potassium benzyloxide

  • 122-78-1
    122-78-1

    phenylacetaldehyde

  • 100-51-6
    100-51-6

    benzyl alcohol

  • 60-12-8
    60-12-8

    2-phenylethanol

3536-29-6 Downstream products

  • 3412-44-0
    3412-44-0

    1,3-diphenylpropene

  • 948-97-0
    948-97-0

    2,3-diphenyl-1-propene

  • 858010-45-4
    858010-45-4

    1-bromo-2,3-diphenyl-propane

  • 38321-63-0
    38321-63-0

    Thiobenzoesaeure-O-2,3-diphenylpropylester

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