2-tert-Butyl-1,3-dithiolane

Base Information

Chemical Name:2-tert-Butyl-1,3-dithiolane
CAS No.:37754-55-5
Molecular Formula:C7H14S2
Molecular Weight:162.3161
Hs Code.:
DSSTox Substance ID:DTXSID60191201
Nikkaji Number:J91.140B
Wikidata:Q83063705

Synonyms:2-tert-Butyl-1,3-dithiolane;1,3-DITHIOLANE, 2-tert-BUTYL-;BRN 1421175;37754-55-5;5-19-01-00106 (Beilstein Handbook Reference);SCHEMBL10050826;DTXSID60191201;LS-63234;1,3-dithiolane, 2-(1,1-dimethylethyl)-;InChI=1/C7H14S2/c1-7(2,3)6-8-4-5-9-6/h6H,4-5H2,1-3H

Suppliers and Price of 2-tert-Butyl-1,3-dithiolane

Supply Marketing:

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

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Chemical Property of 2-tert-Butyl-1,3-dithiolane

Chemical Property:

Vapor Pressure:0.193mmHg at 25°C
Boiling Point:217.7°Cat760mmHg
Flash Point:80.2°C
Density:1.054g/cm³
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:162.05369279
Heavy Atom Count:9
Complexity:87.6

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)C1SCCS1

Technology Process of 2-tert-Butyl-1,3-dithiolane

There total 3 articles about 2-tert-Butyl-1,3-dithiolane 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: 45.0%

: 540-63-6
ethane-1,2-dithiol

: 630-19-3
pivalaldehyde

: 37754-55-5
2-(t-butyl)-1,3-dithiolane

Guidance literature:

Reference yield: 10.0%

: 117203-47-1
Dithiopivalinsaeure-(2-chlorethyl)ester

: 37754-55-5
2-(t-butyl)-1,3-dithiolane

Guidance literature:: With tetraethylammonium bromide; In methanol; electroreduction;

Reference yield:

: 117226-30-9
sodium 2,2-dimethylpropanedithioate

: 37754-55-5
2-(t-butyl)-1,3-dithiolane

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / (BzNMe₃)Cl / CHCl₃; H₂O / Ambient temperature

2: 10 percent / 0.2M (NEt₄)Br / methanol / electroreduction

With {N(CH₃)3Bz}Cl; tetraethylammonium bromide; In methanol; chloroform; water;