2-Naphthol, 1,6-dimethyl-

Base Information

Chemical Name:2-Naphthol, 1,6-dimethyl-
CAS No.:17324-10-6
Molecular Formula:C12H12O
Molecular Weight:172.2231
Hs Code.:
European Community (EC) Number:853-887-9
DSSTox Substance ID:DTXSID60169561
Nikkaji Number:J2.806.325C
Wikidata:Q83039279

Synonyms:2-Naphthol, 1,6-dimethyl-;1,6-dimethylnaphthalen-2-ol;17324-10-6;1,6-Dimethyl-2-naphthol;2-Naphthalenol, 1,6-dimethyl-;1,6-Dimethylnaphthalene-2-ol;SCHEMBL13964538;DTXSID60169561;EN300-8235037;Z1513824724

Suppliers and Price of 2-Naphthol, 1,6-dimethyl-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-Naphthol, 1,6-dimethyl-

Chemical Property:

Vapor Pressure:0.000159mmHg at 25°C
Boiling Point:321.4°C at 760 mmHg
Flash Point:154.9°C
Density:1.114g/cm³
XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:172.088815002
Heavy Atom Count:13
Complexity:178

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C=C1)C(=C(C=C2)O)C

Technology Process of 2-Naphthol, 1,6-dimethyl-

There total 6 articles about 2-Naphthol, 1,6-dimethyl- 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:

: 17580-40-4
1,6-Dimethyl-2-methoxy-naphthalin

: 17324-10-6
1,6-Dimethyl-[2]naphthol

Guidance literature:: With hydrogen bromide; In acetic acid;

Reference yield:

: 93-04-9
2-Methoxynaphthalene

: 17324-10-6
1,6-Dimethyl-[2]naphthol

Guidance literature:: Multi-step reaction with 4 steps

1: (i) (formylation), (ii) Zn-Hg, aq. HCl

2: aq. HCl

3: Zn, AcOH

4: aq. HBr / acetic acid

With hydrogenchloride; hydrogen bromide; acetic acid; zinc; In acetic acid;

Reference yield:

: 1130-80-9
2-methoxy-1-methylnaphthalene

: 17324-10-6
1,6-Dimethyl-[2]naphthol

Guidance literature:: Multi-step reaction with 3 steps

1: aq. HCl

2: Zn, AcOH

3: aq. HBr / acetic acid

With hydrogenchloride; hydrogen bromide; acetic acid; zinc; In acetic acid;