Naphthalene, 1-[(phenylmethyl)thio]-

Base Information

Chemical Name:Naphthalene, 1-[(phenylmethyl)thio]-
CAS No.:5023-64-3
Molecular Formula:C17H14S
Molecular Weight:250.364
Hs Code.:
DSSTox Substance ID:DTXSID10446152
Nikkaji Number:J1.546.658H
Wikidata:Q82264739

Synonyms:Naphthalene, 1-[(phenylmethyl)thio]-;5023-64-3;1-Naphthylbenzyl sulfide;Benzyl(naphthalen-1-yl)sulfane;SCHEMBL6057233;DTXSID10446152;DCDUWZAHMMXKRE-UHFFFAOYSA-N

Suppliers and Price of Naphthalene, 1-[(phenylmethyl)thio]-

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 3 raw suppliers

Chemical Property of Naphthalene, 1-[(phenylmethyl)thio]-

Chemical Property:

XLogP3:5.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:250.08162162
Heavy Atom Count:18
Complexity:244

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CSC2=CC=CC3=CC=CC=C32

Technology Process of Naphthalene, 1-[(phenylmethyl)thio]-

There total 20 articles about Naphthalene, 1-[(phenylmethyl)thio]- 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: 100.0%

: 90-11-9
1-Bromonaphthalene

: 100-53-8
phenylmethanethiol

: 5023-64-3
1-(benzylsulfanyl)naphthalene

Guidance literature:: phenylmethanethiol; With sodium t-butanolate; In tetrahydrofuran; at 23 ℃; for 0.166667h; Inert atmosphere;

With zinc(II) chloride; In tetrahydrofuran; for 0.166667h; Inert atmosphere;

1-Bromonaphthalene; With di-μ-bromobis(tri-tert-butylphosphino)dipalladium(I); lithium iodide; In tetrahydrofuran; at 90 ℃; for 2h; Inert atmosphere;
DOI:10.1021/jo900385d

Reference yield: 97.0%

: 90-14-2
1-Iodonaphthalene

: 100-53-8
phenylmethanethiol

: 5023-64-3
1-(benzylsulfanyl)naphthalene

Guidance literature:: With tetra(n-butyl)ammonium hydroxide; In water; at 50 ℃; for 24h; chemoselective reaction; Inert atmosphere; Sealed tube;
DOI:10.1039/c2ob06795a

Reference yield: 96.0%

: 18506-73-5
1-(benzylsulfinyl)naphthalene

: 5023-64-3
1-(benzylsulfanyl)naphthalene

Guidance literature:: With trifluoromethylsulfonic anhydride; potassium iodide; In acetonitrile; at 20 ℃; for 0.05h;
DOI:10.1055/s-2008-1067190