2-Mercapto-4,6-di-tert-butylphenol

Base Information

Chemical Name:2-Mercapto-4,6-di-tert-butylphenol
CAS No.:53551-74-9
Molecular Formula:C14H22OS
Molecular Weight:238.394
Hs Code.:
DSSTox Substance ID:DTXSID10201763
Nikkaji Number:J3.493.574B
Wikidata:Q83074982
Mol file:53551-74-9.mol

Synonyms:2-Mercapto-4,6-di-tert-butylphenol;53551-74-9;2,4-ditert-butyl-6-sulfanylphenol;2,4-di-tert-butyl-6-mercaptophenol;Phenol, 2,4-di-tert-butyl-6-mercapto-;4,6-Di-tert-butyl-2-mercaptophenol;Phenol, 2,2-bis(1,1-dimethylethyl)-6-mercapto-;2,2-Bis(1,1-dimethylethyl)-6-mercaptophenol;starbld0020617;SCHEMBL1685565;DTXSID10201763;SEUXZGMOSAXITB-UHFFFAOYSA-N;3,5-di-t-butyl-2-hydroxythiophenol;AKOS030240240;LS-104065;J3.493.574B

Suppliers and Price of 2-Mercapto-4,6-di-tert-butylphenol

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

TRC
2-Mercapto-4,6-di-tert-butylphenol
1g
$ 1320.00

Medical Isotopes, Inc.
2-Mercapto-4,6-di-tert-butylphenol
100 mg
$ 650.00

Total 5 raw suppliers

Chemical Property of 2-Mercapto-4,6-di-tert-butylphenol

Chemical Property:

Vapor Pressure:0.000836mmHg at 25°C
Boiling Point:296°Cat760mmHg
Flash Point:132.8°C
Density:1.019g/cm³
Solubility.:Dichloromethane, Diethyl Ether, Hexanes
XLogP3:5.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:238.13913649
Heavy Atom Count:16
Complexity:236

Purity/Quality:

99% ^*data from raw suppliers

2-Mercapto-4,6-di-tert-butylphenol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1=CC(=C(C(=C1)S)O)C(C)(C)C
Uses 2-Mercapto-4,6-di-tert-butylphenol (cas# 53551-74-9) is a compound useful in organic synthesis.

Technology Process of 2-Mercapto-4,6-di-tert-butylphenol

There total 2 articles about 2-Mercapto-4,6-di-tert-butylphenol 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: 97.0%

: 40026-99-1
2,2'-trithiobis(4,6-t-butylphenol)

: 53551-74-9
3,5-di-tert-butyl-2-hydroxybenzenethiol

Guidance literature:: With hydrogenchloride; zinc; In ethanol; toluene; for 48h;

Reference yield:

: 96-76-4
2,4-di-tert-Butylphenol

: 53551-74-9
3,5-di-tert-butyl-2-hydroxybenzenethiol

Guidance literature:: With hydrogenchloride; disulfur dichloride; zinc; Yield given. Multistep reaction; 1.) benzene, 40-45 deg C, 2.) benzene, 75-80 deg C, 24 h;