• Chemical Name 4-(p-hydroxyphenyl)butan-2-ol
  • CAS No. 69617-84-1
  • Contact Us Inquiry

Factory Sells Best Quality 4-(p-hydroxyphenyl)butan-2-ol 69617-84-1 with ISO standards

  • Molecular Formula: C10H14 O2
  • Molecular Weight: 166.22
  • Vapor Pressure: 0.000186mmHg at 25°C 
  • Melting Point: 71℃ (ethanol ) 
  • Boiling Point: 315.4°C at 760 mmHg 
  • PKA: 10.12±0.15(Predicted) 
  • Flash Point: 153.4°C 
  • PSA: 40.46000 
  • Density: 1.096g/cm3 
  • LogP: 1.70560 

4-(p-hydroxyphenyl)butan-2-ol(Cas 69617-84-1) Usage

InChI:InChI=1/C10H14O2/c1-8(11)2-3-9-4-6-10(12)7-5-9/h4-8,11-12H,2-3H2,1H3

69617-84-1 Relevant articles

Enzymatic production of both enantiomers of rhododendrol

Musa, Musa M.

, p. 6719 - 6721 (2014)

An asymmetric synthetic approach to prod...

Deracemization and Stereoinversion of Alcohols Using Two Mutants of Secondary Alcohol Dehydrogenase from Thermoanaerobacter pseudoethanolicus

Hamdan, Samir M.,Musa, Musa M.,Nafiu, Sodiq A.,Takahashi, Etsuko,Takahashi, Masateru

, (2020/07/24)

We developed a one-pot sequential two-st...

Expanding the Substrate Specificity of Thermoanaerobacter pseudoethanolicus Secondary Alcohol Dehydrogenase by a Dual Site Mutation

Musa, Musa M.,Bsharat, Odey,Karume, Ibrahim,Vieille, Claire,Takahashi, Masateru,Hamdan, Samir M.

, p. 798 - 805 (2018/02/21)

Here, we report the asymmetric reduction...

Selective hydrogenation of conjugated unsaturated ketones containing a hydroxyaryl substituent in the β-position

Kovalenko,Pratsko

, p. 24 - 28 (2017/03/16)

A high selectivity was achieved in the N...

Deracemization of Secondary Alcohols by using a Single Alcohol Dehydrogenase

Karume, Ibrahim,Takahashi, Masateru,Hamdan, Samir M.,Musa, Musa M.

, p. 1459 - 1463 (2016/05/02)

We developed a single-enzyme-mediated tw...

69617-84-1 Process route

4-(4-hydroxyphenyl)-2-oxobutane
5471-51-2

4-(4-hydroxyphenyl)-2-oxobutane

rac-rhododendrol
69617-84-1

rac-rhododendrol

Conditions
Conditions Yield
With sodium tetrahydroborate; In methanol; at 20 ℃; for 2h; Solvent; Enzymatic reaction;
100%
With sodium tetrahydroborate; In methanol; at 0 - 20 ℃; for 1.5h; Inert atmosphere;
95%
With sodium tetrahydroborate; In methanol; water; at 20 ℃; for 10h; Cooling with ice;
94%
With sodium tetrahydroborate; In methanol; at 20 ℃; for 19h;
92%
With sodium tetrahydroborate; In ethanol; at 20 ℃; for 2h;
90%
With lithium aluminium tetrahydride; In tetrahydrofuran; for 48h; Heating;
With nickel boride; hydrogen; In methanol; at 25 ℃; for 18h;
1 g
With sodium tetrahydroborate;
With sodium tetrahydroborate;
(E)-4-(4-hydroxyphenyl)-3-buten-2-one
22214-30-8

(E)-4-(4-hydroxyphenyl)-3-buten-2-one

rac-rhododendrol
69617-84-1

rac-rhododendrol

4-(4-hydroxyphenyl)-2-oxobutane
5471-51-2

4-(4-hydroxyphenyl)-2-oxobutane

Conditions
Conditions Yield
With sodium tetrahydroborate; nickel(II) chloride hexahydrate; hydrogen; In methanol; at 0 - 30 ℃; under 760.051 Torr; Reagent/catalyst; Solvent; Temperature; Time; Reflux; Inert atmosphere;
98%
1%
With sodium tetrahydroborate; nickel dichloride; In methanol;
38%
61%
With methanol; formic acid; water; silica gel; palladium dichloride; for 12h; Heating;
25%
45%
With baker's yeast; ethanol; D-glucose; water; at 36 ℃; for 92h; Product distribution; var. reducing agents, also labelled;
With formic acid; palladium 10% on activated carbon; ammonium formate; In methanol; at 50 ℃; for 15h;

69617-84-1 Upstream products

  • 168038-86-6
    168038-86-6

    (RS)-rhododendrol 2-O-β-D-glucopyranoside

  • 22214-30-8
    22214-30-8

    (E)-4-(4-hydroxyphenyl)-3-buten-2-one

  • 67-56-1
    67-56-1

    methanol

  • 22214-30-8
    22214-30-8

    4-(4'-hydroxyphenyl)but-3-en-2-one

69617-84-1 Downstream products

  • 67952-38-9
    67952-38-9

    4-(4-methoxy-phenyl)-butan-2-ol

  • 59092-94-3
    59092-94-3

    (+)-rhododendrol

  • 129752-69-8
    129752-69-8

    (R)-(+)-4-(4'-hydroxyphenyl)-2-butyl acetate

  • 85120-75-8
    85120-75-8

    (R)-(+)-4-(4'-acetoxyphenyl)-2-butyl acetate