Naphthalene, 2-[[(phenylmethyl)thio]methyl]-

Base Information

Chemical Name:Naphthalene, 2-[[(phenylmethyl)thio]methyl]-
CAS No.:88766-10-3
Molecular Formula:C18H16S
Molecular Weight:264.391
Hs Code.:
DSSTox Substance ID:DTXSID00415630
Wikidata:Q82224574

Synonyms:ghl.PD_Mitscher_leg0.168;Naphthalene, 2-[[(phenylmethyl)thio]methyl]-;88766-10-3;SCHEMBL1127606;DTXSID00415630

Suppliers and Price of Naphthalene, 2-[[(phenylmethyl)thio]methyl]-

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
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price

Total 1 raw suppliers

Chemical Property of Naphthalene, 2-[[(phenylmethyl)thio]methyl]-

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:264.09727168
Heavy Atom Count:19
Complexity:256

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CSCC2=CC3=CC=CC=C3C=C2

Technology Process of Naphthalene, 2-[[(phenylmethyl)thio]methyl]-

There total 1 articles about Naphthalene, 2-[[(phenylmethyl)thio]methyl]- 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: 77.0%

: 100-53-8
phenylmethanethiol

: 939-26-4
2-bromomethylnaphthyl bromide

: 88766-10-3
2-naphthylmethyl benzyl sulfide

Guidance literature:: With potassium hydroxide; In ethanol; Heating;
DOI:10.1021/ja00318a037

Reference yield:

: 88766-10-3
2-naphthylmethyl benzyl sulfide

: 67168-91-6
2-naphthylmethyl benzyl sulfone

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jo3021852

Reference yield:

: 88766-10-3
2-naphthylmethyl benzyl sulfide

: 2039-70-5,2840-89-3,3132-88-5,85248-68-6,85248-69-7,129446-34-0
(E)-2-styrylnaphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C

2: 1,2-dibromo-1,1,2,2-tetrachloroethane; alumina-supported potassium hydroxide / tetrahydrofuran; tert-butyl alcohol / 8 h / 20 °C

With 1,2-dibromo-1,1,2,2-tetrachloroethane; alumina-supported potassium hydroxide; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; tert-butyl alcohol; 2: |Ramberg-Baecklund Rearrangement;
DOI:10.1021/jo3021852