Disulfide,bis(phenylthioxomethyl)
Product Information
Molecular Formula
C14H10 S4
Molecular Weight
306.4892
Description
Reversible Addition Fragmentation Chain Transfer (RAFT) Polymerization
Synonyms
benzenecarbonothioylsulfanylbenzenecarbodithioate;5873-93-8;thiobenzoyldisulfide;dithiobenzoyldisulfide;Dithiobenzoyldisulphide;di(thiobenzoyl)disulfide
IUPAC Name
benzenecarbonothioylsulfanyl benzenecarbodithioate
SMILES
C1=CC=C(C=C1)C(=S)SSC(=S)C2=CC=CC=C2
InChI
InChI=1S/C14H10S4/c15-13(11-7-3-1-4-8-11)17-18-14(16)12-9-5-2-6-10-12/h1-10H
InChI Key
LWGLGSPYKZTZBM-UHFFFAOYSA-N
Boiling Point
446.8°C at 760 mmHg
Melting Point
89.0 to 93.0 °C
Flash Point
>230 °F
Purity
95%
Density
1.367 g/cm3
Appearance
White to Brown to Dark purple powder to crystal
Storage
−20°C
Safety Information
Hazards
H413:
May cause long-lasting harmful effects to aquatic life.
May cause long-lasting harmful effects to aquatic life.
Precautionary Statement
P273:
Avoid release to the environment.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.
Avoid release to the environment.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.
Computed Properties
XLogP3
5
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
5
Exact Mass
305.96653501 g/mol
Monoisotopic Mass
305.96653501 g/mol
Topological Polar Surface Area
115Ų
Heavy Atom Count
18
Formal Charge
0
Complexity
258
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-112480061-A | Method for preparing vinylene carbonate by using waste | 2020-12-27 |
| JP-6933288-B1 | Varnish for active energy ray-curable ink, active energy ray-curable ink, and printed matter | 2020-10-16 |
| JP-2022039516-A | Method for producing bis (thiocarbonyl) disulfide compound | 2020-08-28 |
| JP-2022035155-A | Image forming method and image forming device | 2020-08-20 |
| JP-2022035200-A | Inkjet ink and image formation method | 2020-08-20 |
| JP-2022030910-A | How to clean the ink ejection part of the inkjet head | 2020-08-07 |
| US-2022040980-A1 | Method for cleaning ink discharger of inkjet head | 2020-08-07 |
| JP-2022016981-A | Image formation method | 2020-07-13 |
| WO-2022006703-A1 | Composition, coating formulation, and multilayer body | 2020-07-06 |
| JP-2022006905-A | Active energy ray-curable ink for lithographic offset printing and its manufacturing method | 2020-06-25 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 22628191 | 2012-08-14 | From NMP to RAFT and thiol-ene chemistry by in situ functionalization of nitroxide chain ends | Macromolecular rapid communications |
