3-Chloro-4-methylbenzyl alcohol

Base Information

• Chemical Name: 3-Chloro-4-methylbenzyl alcohol
• CAS No.: 39652-32-9
• Molecular Formula: C8H9ClO
• Molecular Weight: 156.612
• Hs Code.: 2906299090
• European Community (EC) Number: 254-566-0
• DSSTox Substance ID: DTXSID70192764
• Nikkaji Number: J261.415D
• Wikidata: Q83065425
• Mol file: 39652-32-9.mol

Synonyms:3-Chloro-4-methylbenzyl alcohol;39652-32-9;(3-Chloro-4-methylphenyl)methanol;3-Chloro-4-methylbenzenemethanol;EINECS 254-566-0;Benzenemethanol, 3-chloro-4-methyl-;SCHEMBL92958;DTXSID70192764;MFCD00016863;(3-Chloro-4-methylphenyl)methanol #;AKOS009461310;3-Chloro-4-methylbenzyl Alcohol, Tech.;BS-23093;3-Chloro-4-methylbenzyl alcohol, AldrichCPR;CS-0194513;FT-0615418;A22590;E89334;EN300-748865

Chemical Property of 3-Chloro-4-methylbenzyl alcohol

Chemical Property:

• Appearance/Colour: liquid
• Vapor Pressure: 0.0103mmHg at 25°C
• Refractive Index: 1.558
• Boiling Point: 252.1 °C at 760 mmHg
• Flash Point: 106.3 °C
• PSA: 20.23000
• Density: 1.191 g/cm³
• LogP: 2.14070
• XLogP3: 2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 156.0341926
• Heavy Atom Count: 10
• Complexity: 105

Purity/Quality:

97% ^*data from raw suppliers

3-Chloro-4-methylbenzylAlcohol ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C=C(C=C1)CO)Cl
• Uses: It is used in the synthesis of heterocycles on the basis of arylation products of unsaturated compounds.

Technology Process of 3-Chloro-4-methylbenzyl alcohol

There total 4 articles about 3-Chloro-4-methylbenzyl alcohol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

3-chloro-4-methylbenzoic acid (5162-82-3) → (3-chloro-4-methylphenyl) methanol (39652-32-9)

Guidance literature:

With borane-THF; In tetrahydrofuran; at 0 - 20 ℃;

Reference yield:

{2-chloro-4-[(phenylmethyl)oxy]phenyl}methanol (219764-60-0) → (3-chloro-4-methylphenyl) methanol (39652-32-9)

Guidance literature:

Reference yield:

3-Chlor-4-methyl-benzaldehyd (3411-03-8) → 3-chloro-4-methylbenzoic acid (5162-82-3) + (3-chloro-4-methylphenyl) methanol (39652-32-9)

Guidance literature:

With potassium hydroxide;

upstream raw materials:

3-Chlor-4-methyl-benzaldehyd

3-chloro-4-methylbenzoic acid

{2-chloro-4-[(phenylmethyl)oxy]phenyl}methanol

Downstream raw materials:

3-chloro-4-methylbenzamide

1,3-bis(3-chloro-4-methylphenyl)urea

3-chloro-4-methylbenzonitrile

1-methyl-2-chloro-4-chloromethylbenzene

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