Cas no 13616-83-6 (Bis(2,4-dimethylphenyl) Disulfide)
Bis(2,4-dimethylphenyl) Disulfide Chemical and Physical Properties
Names and Identifiers
-
- Disulfide,bis(2,4-dimethylphenyl)
- (2,4-XYLYL)DISULPHIDE
- 2,4-Xylyl disulfide
- AC1L35SO
- bis(2,4-dimethylphenyl) disulfide
- Bis-(2,4-dimethyl-phenyl)-disulfid
- bis-(2,4-dimethyl-phenyl)-disulfide
- Bis-< 2,4-dimethyl-phenyl> -disulfid
- CTK4C0205
- di(2,4-xylyl) disulfide
- Di(2,4-xylyl) disulphide
- EINECS 237-101-6
- PubChem15314
- Vortioxetine impurity H
- Vortioxetine Impurity 18
- Bis(2,4-xylyl) persulfide
- SCHEMBL576257
- BS-53300
- 1,2-bis(2,4-dimethylphenyl)disulfane
- NS00024412
- AKOS028108525
- Disulfide, bis(2,4-dimethylphenyl)
- Dixylyl disulphide
- DTXSID0065561
- J-520407
- UNII-534Y509F25
- Q27896341
- 13616-83-6
- F75563
- DIXYLYLDISULPHIDE
- Di(2,4-xylyl)disulphide
- EN300-18564213
- Bis(2,4-xylyl) disulfide
- 1-[(2,4-dimethylphenyl)disulfanyl]-2,4-dimethylbenzene
- 534Y509F25
- RPYHJOQRKNEXCU-UHFFFAOYSA-N
- 2,4-Xylyl disulfide (6CI,7CI,8CI);1,2-Bis(2,4-dimethylphenyl)disulfane;
- Bis(2,4-dimethylphenyl) Disulfide
-
- Inchi： 1S/C16H18S2/c1-11-5-7-15(13(3)9-11)17-18-16-8-6-12(2)10-14(16)4/h5-10H,1-4H3
- InChI Key： RPYHJOQRKNEXCU-UHFFFAOYSA-N
- SMILES： S(C1C=CC(C)=CC=1C)SC1C=CC(C)=CC=1C
Computed Properties
- Exact Mass: 274.08514
- Monoisotopic Mass: 274.084992
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 18
- Rotatable Bond Count: 3
- Complexity: 228
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 50.6
- XLogP3: 5.5
Experimental Properties
- Density: 1.13±0.1 g/cm3 (20 oC 760 Torr),
- Melting Point: 265 oC
- Boiling Point: 365.1°Cat760mmHg
- Flash Point: 174.6°C
- Refractive Index: 1.628
- Solubility: Insuluble (6.0E-5 g/L) (25 oC),
- PSA: 0
Bis(2,4-dimethylphenyl) Disulfide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | D488660-10mg |
Bis(2,4-dimethylphenyl) Disulfide |
13616-83-6 | 10mg |
$ 57.00 | 2023-09-07 | ||
| TRC | D488660-50mg |
Bis(2,4-dimethylphenyl) Disulfide |
13616-83-6 | 50mg |
$ 91.00 | 2023-09-07 | ||
| TRC | D488660-100mg |
Bis(2,4-dimethylphenyl) Disulfide |
13616-83-6 | 100mg |
$ 132.00 | 2023-09-07 | ||
| Crysdot LLC | CD12149891-1g |
1,2-Bis(2,4-dimethylphenyl)disulfane |
13616-83-6 | 97% | 1g |
$250 | 2024-07-18 | |
| Crysdot LLC | CD12149891-5g |
1,2-Bis(2,4-dimethylphenyl)disulfane |
13616-83-6 | 97% | 5g |
$750 | 2024-07-18 | |
| A2B Chem LLC | AD27859-100mg |
Disulfide,bis(2,4-dimethylphenyl) |
13616-83-6 | 97% | 100mg |
$79.00 | 2024-04-20 | |
| A2B Chem LLC | AD27859-250mg |
Disulfide,bis(2,4-dimethylphenyl) |
13616-83-6 | 97% | 250mg |
$127.00 | 2024-04-20 | |
| A2B Chem LLC | AD27859-1g |
Disulfide,bis(2,4-dimethylphenyl) |
13616-83-6 | 97% | 1g |
$325.00 | 2024-04-20 | |
| A2B Chem LLC | AD27859-5g |
Disulfide,bis(2,4-dimethylphenyl) |
13616-83-6 | 97% | 5g |
$1111.00 | 2024-04-20 | |
| eNovation Chemicals LLC | Y1333592-250mg |
Disulfide,bis(2,4-dimethylphenyl) |
13616-83-6 | 97% | 250mg |
$150 | 2023-09-04 |
Bis(2,4-dimethylphenyl) Disulfide Related Literature
-
Wei-Ching Chen,Rekha Bai,Wan-Lin Cheng,Chun-Yu Peng,Daggula Mallikarjuna Reddy,Satpal Singh Badsara,Chin-Fa Lee Org. Biomol. Chem. 2023 21 3002
Additional information on Bis(2,4-dimethylphenyl) Disulfide
Recent Advances in the Study of Bis(2,4-dimethylphenyl) Disulfide (CAS: 13616-83-6) in Chemical Biology and Pharmaceutical Research
Bis(2,4-dimethylphenyl) disulfide (CAS: 13616-83-6) is an organic disulfide compound that has garnered significant attention in recent years due to its potential applications in chemical biology and pharmaceutical research. This compound, characterized by its unique molecular structure, has been investigated for its role in various biochemical processes, including redox reactions, enzyme inhibition, and as a precursor in the synthesis of more complex molecules. The growing body of research on this compound underscores its importance in advancing our understanding of disulfide chemistry and its therapeutic potential.
Recent studies have focused on elucidating the mechanistic pathways through which Bis(2,4-dimethylphenyl) disulfide interacts with biological systems. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that this compound exhibits potent inhibitory effects on certain cysteine proteases, which are implicated in a range of diseases, including cancer and neurodegenerative disorders. The study employed X-ray crystallography and molecular docking simulations to reveal the binding modes of the disulfide to the active sites of these enzymes, providing valuable insights for drug design.
In addition to its role as an enzyme inhibitor, Bis(2,4-dimethylphenyl) disulfide has been explored for its utility in material science and nanotechnology. A recent report in ACS Applied Materials & Interfaces highlighted its use as a stabilizing agent in the synthesis of metal nanoparticles, where it effectively prevents aggregation and enhances the nanoparticles' catalytic properties. This dual functionality—both in biological and material applications—positions the compound as a versatile tool for interdisciplinary research.
Despite these promising findings, challenges remain in optimizing the compound's bioavailability and minimizing potential toxicity. A 2022 review in Chemical Research in Toxicology summarized the current understanding of the compound's metabolic pathways and identified key areas for future research, such as the development of derivatives with improved pharmacokinetic profiles. These efforts are critical for translating laboratory findings into clinically viable therapeutics.
In conclusion, Bis(2,4-dimethylphenyl) disulfide (CAS: 13616-83-6) represents a compelling area of study in chemical biology and pharmaceutical research. Its diverse applications, from enzyme inhibition to nanotechnology, underscore its potential to drive innovation in multiple fields. Continued research into its mechanisms of action and therapeutic potential will be essential for unlocking its full value in both academic and industrial settings.
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