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1-(p-Chlorophenyl)-3-(5-chloro-2-hydroxyphenyl)propan-1-ol

  • CAS 93962-67-5
  • Purity 99%
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Cost-effective customized wholesale 1-(p-Chlorophenyl)-3-(5-chloro-2-hydroxyphenyl)propan-1-ol 93962-67-5

  • Molecular Formula: C15H14Cl2O2
  • Molecular Weight: 297.181
  • Vapor Pressure: 6.42E-09mmHg at 25°C 
  • Boiling Point: 450.9°C at 760 mmHg 
  • Flash Point: 226.5°C 
  • PSA： 40.46000 
  • Density: 1.35g/cm3 
  • LogP: 4.36520 

1-(p-Chlorophenyl)-3-(5-chloro-2-hydroxyphenyl)propan-1-ol(Cas 93962-67-5) Usage

Category

Synthetic organic compound
It is artificially synthesized and belongs to the class of organic compounds.

Chirality

Chiral compound with two chiral centers
The compound has two centers of asymmetry, which means it can exist in different stereoisomers.

Derivative

Phenylpropanol
It is derived from the parent compound phenylpropanol, which is a type of alcohol.

Structural groups

p-chlorophenyl and 5-chloro-2-hydroxyphenyl
The compound contains two distinct functional groups, which are responsible for its chemical properties.

Potential applications

Pharmaceutical industry
It may be used as an intermediate in the synthesis of other chemical compounds, particularly in the pharmaceutical sector.

Research and development

Ongoing
Further research is needed to fully understand its specific properties and potential uses.

Solubility

Unknown (requires experimental data)
The solubility of the compound in various solvents is not provided and would need to be determined through experimentation.

Stability

Unknown (requires experimental data)
The stability of the compound under different conditions is not provided and would need to be determined through experimentation.

Reactivity

Unknown (requires experimental data)
The reactivity of the compound with other substances is not provided and would need to be determined through experimentation.

General Description

1-(p-Chlorophenyl)-3-(5-chloro-2-hydroxyphenyl)propan-1-ol is a chemical compound with the molecular formula C15H15Cl2O2. It is a synthetic organic compound, which is categorized as a chiral compound with two chiral centers. 1-(p-Chlorophenyl)-3-(5-chloro-2-hydroxyphenyl)propan-1-ol is a derivative of phenylpropanol and contains both p-chlorophenyl and 5-chloro-2-hydroxyphenyl groups. It has potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of other chemical compounds. Its specific properties and potential uses are subject to further research and development.

InChI:InChI=1/C15H14Cl2O2/c16-12-4-1-10(2-5-12)14(18)7-3-11-9-13(17)6-8-15(11)19/h1-2,4-6,8-9,14,18-19H,3,7H2

93962-67-5 Relevant articles

A Modular Synthesis of 2-Alkyl- and 2-Arylchromans via a Three-Step Sequence

Orr, Robert K.,Campeau, Louis-Charles,Chobanian, Harry R.,McCabe Dunn, Jamie M.,Pio, Barbara,Plummer, Christopher W.,Nolting, Andrew,Ruck, Rebecca T.

, p. 657 - 666 (2017)

A convergent three-step method for the s...

93962-67-5 Process route

3-(5-chloro-2-hydroxyphenyl)-1-(4-chlorophenyl)propan-1-one
93962-68-6

3-(5-chloro-2-hydroxyphenyl)-1-(4-chlorophenyl)propan-1-one

C<sub>15</sub>H<sub>14</sub>Cl<sub>2</sub>O<sub>2</sub>
93962-67-5

C15 H14 Cl2 O2

Conditions
Conditions Yield
With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 - 20 ℃; for 1h;
p-chlorophenylvinylcarbinol
58824-54-7

p-chlorophenylvinylcarbinol

C<sub>15</sub>H<sub>14</sub>Cl<sub>2</sub>O<sub>2</sub>
93962-67-5

C15 H14 Cl2 O2

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: t-BuXPhos palladacycle Gen 2; N-Methyldicyclohexylamine / toluene / 1 h / 100 °C / Inert atmosphere
2: sodium tetrahydroborate / tetrahydrofuran; methanol / 1 h / 0 - 20 °C
With sodium tetrahydroborate; N-Methyldicyclohexylamine; t-BuXPhos palladacycle Gen 2; In tetrahydrofuran; methanol; toluene; 1: |Heck Reaction;

93962-67-5 Upstream products

  • 58824-54-7
    58824-54-7

    p-chlorophenylvinylcarbinol

  • 71643-66-8
    71643-66-8

    4-chloro-2-iodo phenol

  • 93962-68-6
    93962-68-6

    3-(5-chloro-2-hydroxyphenyl)-1-(4-chlorophenyl)propan-1-one

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