(2-Chlorophenyl)(naphthalen-1-yl)methanol

Base Information

• Chemical Name: (2-Chlorophenyl)(naphthalen-1-yl)methanol
• CAS No.: 42074-40-8
• Molecular Formula: C17H13ClO
• Molecular Weight: 268.7375
• NSC Number: 99463
• DSSTox Substance ID: DTXSID20295057

Synonyms:(2-chlorophenyl)(naphthalen-1-yl)methanol;42074-40-8;NSC99463;NCIOpen2_006679;DTXSID20295057;NSC-99463;(2-chlorophenyl)(1-naphthyl)methanol;AKOS003583851;AKOS017481476

Chemical Property of (2-Chlorophenyl)(naphthalen-1-yl)methanol

Chemical Property:

• Vapor Pressure: 1.68E-08mmHg at 25°C
• Boiling Point: 439.5°Cat760mmHg
• Flash Point: 219.6°C
• Density: 1.26g/cm³
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 268.0654927
• Heavy Atom Count: 19
• Complexity: 293

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C=CC=C2C(C3=CC=CC=C3Cl)O

Technology Process of (2-Chlorophenyl)(naphthalen-1-yl)methanol

There total 2 articles about (2-Chlorophenyl)(naphthalen-1-yl)methanol 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:

1-Bromonaphthalene (90-11-9) + 2-chloro-benzaldehyde (89-98-5) → (2-chloro-phenyl)-[1]naphthyl-methanol (42074-40-8)

Guidance literature:

Multistep reaction; (i) Mg, Et₂O, (ii) /BRN= 385877/, benzene;

DOI:10.1002/jps.2600620514

Reference yield:

2-chloro-benzaldehyde (89-98-5) + 1-naphthylmagnesiumbromide (703-55-9) → (2-chloro-phenyl)-[1]naphthyl-methanol (42074-40-8)

Guidance literature:

With diethyl ether;

DOI:10.1021/ja01148a600

Reference yield: 91.0%

(2-chloro-phenyl)-[1]naphthyl-methanol (42074-40-8) → (chloro(2-chlorophenyl)methyl)naphthalene (42074-49-7)

Guidance literature:

With thionyl chloride; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1021/ja300164d

upstream raw materials:

2-chloro-benzaldehyde

1-naphthylmagnesiumbromide

1-Bromonaphthalene

Downstream raw materials:

(chloro(2-chlorophenyl)methyl)naphthalene

4-(4-(2-chlorobenzyl)naphthalen-1-yl)morpholine

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