o-(2-Naphthyl)phenol

Base Information

Chemical Name:o-(2-Naphthyl)phenol
CAS No.:78210-35-2
Molecular Formula:C16H12 O
Molecular Weight:220.271
Hs Code.:2907199090
European Community (EC) Number:278-871-3
DSSTox Substance ID:DTXSID20999447
Nikkaji Number:J319.740I
Wikidata:Q82992485
ChEMBL ID:CHEMBL4455327
Mol file:78210-35-2.mol

Synonyms:78210-35-2;o-(2-Naphthyl)phenol;2-(NAPHTHALEN-2-YL)PHENOL;2-naphthalen-2-ylphenol;2-(2-Hydroxyphenyl)naphthalene;EINECS 278-871-3;ss-Naphthylphenol;2-(2-naphthyl)phenol;SCHEMBL217638;CHEMBL4455327;DTXSID20999447;MFCD18312884;AKOS017557815;BS-29617;CS-0209312

Suppliers and Price of o-(2-Naphthyl)phenol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
2-(2-Hydroxyphenyl)naphthalene 95+%
5g
$ 752.00

Chemenu
2-(2-Hydroxyphenyl)naphthalene 95%
5g
$ 711.00

Alichem
2-(2-Hydroxyphenyl)naphthalene
1g
$ 1600.75

Alichem
2-(2-Hydroxyphenyl)naphthalene
500mg
$ 950.60

Alichem
2-(2-Hydroxyphenyl)naphthalene
250mg
$ 686.80

Total 7 raw suppliers

Chemical Property of o-(2-Naphthyl)phenol

Chemical Property:

Vapor Pressure:2.37E-06mmHg at 25°C
Boiling Point:381.1°C at 760 mmHg
Flash Point:183.4°C
PSA：20.23000
Density:1.176g/cm³
LogP:4.21240
XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:220.088815002
Heavy Atom Count:17
Complexity:250

Purity/Quality:

98%Min ^*data from raw suppliers

2-(2-Hydroxyphenyl)naphthalene 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C=C(C=CC2=C1)C3=CC=CC=C3O

Technology Process of o-(2-Naphthyl)phenol

There total 14 articles about o-(2-Naphthyl)phenol 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: 94.0%

: 580-13-2
2-bromonaphthalene

: 89466-08-0
2-hydroxyphenyl boronic acid

: 78210-35-2
2-(2-hydroxyphenyl)naphthalene

Guidance literature:: With palladium 10% on activated carbon; potassium hydroxide; In ethanol; water; at 150 ℃; for 0.5h; Microwave irradiation;
DOI:10.1002/jhet.2704

Reference yield: 92.0%

: cis-1-ethynyl-2-(2-naphthoyl)cyclopropane

: 78210-35-2
2-(2-hydroxyphenyl)naphthalene

Guidance literature:: With pentacarbonyl(tetrahydrofuran)chromium⁽⁰⁾; triethylamine; In tetrahydrofuran; at 20 ℃; for 6h;
DOI:10.1021/ja017037j

Reference yield: 92.0%

: 533-58-4
2-Iodophenol

: 32316-92-0
naphthalene-2-boronic acid

: 78210-35-2
2-(2-hydroxyphenyl)naphthalene

Guidance literature:: With lithium hydroxide monohydrate; C₂₉H₄₀N₂O₃Pd; In water; N,N-dimethyl-formamide; at 25 ℃; for 24h;
DOI:10.1002/aoc.3778