549312
3,3′-Dihydroxydiphenyl disulfide
97%
Synonym(s):
Bis(3-hydroxyphenyl) disulfide
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
S2(C6H4OH)2
CAS Number:
Molecular Weight:
250.34
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
mp
89-93 °C (lit.)
functional group
disulfide
SMILES string
Oc1cccc(SSc2cccc(O)c2)c1
InChI
1S/C12H10O2S2/c13-9-3-1-5-11(7-9)15-16-12-6-2-4-10(14)8-12/h1-8,13-14H
InChI key
XBNOMKROXZGMFW-UHFFFAOYSA-N
Related Categories
General description
3,3′-Dihydroxydiphenyl disulfide [bis(3-hydroxyphenyl) disulfide] is a symmetrical disulfide derivative that can be prepared by treating 3-hydroxythiophenol with ferric chloride.
Application
3,3′-Dihydroxydiphenyl disulfide may be used in the preparation of bis-[3-(4-fluorobenzyloxy)-phenyl]-disulfide by reacting with 4-fluorobenzyl bromide.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Polar Conjugative Effect of Aryldithia Group on the Dissociation and Ultraviolet Spectra of Substituted Phenols.
Oae S and Yoshihara M.
Bulletin of the Chemical Society of Japan, 41(9), 2082-2086 (1968)
Efficient Route for the Preparation of Benzyloxy-Substituted Benzenesulfonyl Chlorides from Mercaptophenols.
Jumeaux C, et al.
Synthetic Communications, 41(12), 1805-1808 (2011)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service