1-Naphthalen-2-ylsulfanylnaphthalen-2-ol

Base Information

Chemical Name:1-Naphthalen-2-ylsulfanylnaphthalen-2-ol
CAS No.:5432-97-3
Molecular Formula:C20H14OS
Molecular Weight:302.3896
Hs Code.:
NSC Number:29075
DSSTox Substance ID:DTXSID90283002
Nikkaji Number:J2.909.251F
Wikidata:Q82017420

Synonyms:5432-97-3;1-naphthalen-2-ylsulfanylnaphthalen-2-ol;NSC29075;DTXSID90283002;NSC-29075;1-(naphthalen-2-ylthio)naphthalen-2-ol

Suppliers and Price of 1-Naphthalen-2-ylsulfanylnaphthalen-2-ol

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

Total 5 raw suppliers

Chemical Property of 1-Naphthalen-2-ylsulfanylnaphthalen-2-ol

Chemical Property:

Vapor Pressure:7.19E-11mmHg at 25°C
Boiling Point:506.2°Cat760mmHg
Flash Point:245.4°C
Density:1.32g/cm³
XLogP3:6.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:302.07653624
Heavy Atom Count:22
Complexity:371

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C=C(C=CC2=C1)SC3=C(C=CC4=CC=CC=C43)O
General Description 1-(Naphthalen-2-ylsulfanyl)naphthalen-2-ol is a sulfur-substituted naphthol derivative synthesized via condensation reactions involving naphthalen-2-ol and arylthiolate or disulfane reagents, as demonstrated in microwave-assisted and photoinduced substitution methods. 1-(naphthalen-2-ylsulfanyl)naphthalen-2-ol, along with its analogs, has been investigated for potential antimicrobial activity, though specific data on its biological properties are not detailed in the provided abstracts. The synthetic approaches highlight efficient yields and versatility in introducing thioether substituents at the 1-position of 2-naphthol.

Technology Process of 1-Naphthalen-2-ylsulfanylnaphthalen-2-ol

There total 7 articles about 1-Naphthalen-2-ylsulfanylnaphthalen-2-ol 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: 99.0%

: 529-36-2
1-Naphthalenethiol

: 135-19-3
β-naphthol

: 5432-97-3
1-(naphthalen-2-ylthio)naphthalen-2-ol

Guidance literature:: With hydrogen bromide; dimethyl sulfoxide; In chloroform; water; at 100 ℃; for 2h; Green chemistry;
DOI:10.1039/C9NJ00925F