Cas no 52089-10-8 ((3-bromophenyl)(phenyl)sulfane)
(3-bromophenyl)(phenyl)sulfane Chemical and Physical Properties
Names and Identifiers
-
- (3-bromophenyl)(phenyl)sulfane
- 1-BROMO-3-(PHENYLSULFANYL)BENZENE
- G49575
- benzene, 1-bromo-3-(phenylthio)-
- FGPSFZNISIIDND-UHFFFAOYSA-N
- SCHEMBL3285262
- 3-bromophenyl phenyl sulfide
- EN300-3576431
- 52089-10-8
- InChI=1/C12H9BrS/c13-10-5-4-8-12(9-10)14-11-6-2-1-3-7-11/h1-9
- 1-bromo-3-(phenylthio)benzene
-
- Inchi: 1S/C12H9BrS/c13-10-5-4-8-12(9-10)14-11-6-2-1-3-7-11/h1-9H
- InChI Key: FGPSFZNISIIDND-UHFFFAOYSA-N
- SMILES: BrC1=CC=CC(=C1)SC1C=CC=CC=1
Computed Properties
- Exact Mass: 263.96087
- Monoisotopic Mass: 263.96083g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 166
- 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
- XLogP3: 4.7
- Topological Polar Surface Area: 25.3?2
Experimental Properties
- PSA: 0
(3-bromophenyl)(phenyl)sulfane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-3576431-0.05g |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95.0% | 0.05g |
$155.0 | 2025-03-18 | |
| Enamine | EN300-3576431-0.1g |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95.0% | 0.1g |
$232.0 | 2025-03-18 | |
| Enamine | EN300-3576431-0.25g |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95.0% | 0.25g |
$331.0 | 2025-03-18 | |
| Enamine | EN300-3576431-0.5g |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95.0% | 0.5g |
$524.0 | 2025-03-18 | |
| Enamine | EN300-3576431-1.0g |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95.0% | 1.0g |
$671.0 | 2025-03-18 | |
| Enamine | EN300-3576431-2.5g |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95.0% | 2.5g |
$1315.0 | 2025-03-18 | |
| Enamine | EN300-3576431-5.0g |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95.0% | 5.0g |
$1945.0 | 2025-03-18 | |
| Enamine | EN300-3576431-10.0g |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95.0% | 10.0g |
$2884.0 | 2025-03-18 | |
| Aaron | AR023Q10-50mg |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95% | 50mg |
$239.00 | 2025-02-14 | |
| Aaron | AR023Q10-100mg |
1-bromo-3-(phenylsulfanyl)benzene |
52089-10-8 | 95% | 100mg |
$344.00 | 2025-02-14 |
(3-bromophenyl)(phenyl)sulfane Related Literature
-
Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
-
Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang Wang Chem. Commun., 2012,48, 802-804
-
Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
-
Hamid Heydari,Mohammad B. Gholivand New J. Chem., 2017,41, 237-244
Additional information on (3-bromophenyl)(phenyl)sulfane
The Compound CAS No 52089-10-8: (3-Bromophenyl)(Phenyl)Sulfane
(3-Bromophenyl)(Phenyl)Sulfane, identified by the CAS registry number 52089-10-8, is a sulfur-containing organic compound that has garnered significant attention in the fields of organic chemistry and materials science. This compound is a derivative of thiophene, a heterocyclic compound with a five-membered ring consisting of four carbon atoms and one sulfur atom. The structure of (3-Bromophenyl)(Phenyl)Sulfane features a bromine atom at the third position of one phenyl ring, which introduces unique electronic and steric properties to the molecule.
Recent studies have highlighted the potential of (3-Bromophenyl)(Phenyl)Sulfane in various applications, particularly in the synthesis of advanced materials. Its ability to undergo sulfur-based coupling reactions has made it a valuable precursor in the development of novel polymers and coordination compounds. For instance, researchers have utilized this compound to synthesize metallopolymers with enhanced mechanical and thermal stability, which hold promise for use in high-performance materials.
The synthesis of (3-Bromophenyl)(Phenyl)Sulfane typically involves the reaction of 3-bromothiophenol with phenol under specific conditions. This reaction pathway is optimized to ensure high yield and purity, making it suitable for large-scale production. The compound's stability under various environmental conditions has also been extensively studied, revealing its resistance to oxidation and hydrolysis, which are critical factors for its practical applications.
In terms of spectroscopic analysis, (3-Bromophenyl)(Phenyl)Sulfane exhibits distinct absorption bands in the UV-vis spectrum due to its conjugated system. These spectral characteristics are being exploited in the development of sensors and optical devices. Recent advancements in computational chemistry have also enabled detailed quantum mechanical modeling of this compound, providing deeper insights into its electronic structure and reactivity.
The integration of (3-Bromophenyl)(Phenyl)Sulfane into nanotechnology applications is another area of active research. Its ability to form self-assembled monolayers on various substrates has been leveraged to create nanoscale devices with tailored functionalities. For example, researchers have demonstrated the use of this compound in constructing molecular switches and memory devices, showcasing its potential in next-generation electronics.
In conclusion, (3-Bromophenyl)(Phenyl)Sulfane (CAS No 52089-10-8) stands as a versatile building block in modern chemistry. Its unique properties and diverse applications continue to drive innovative research across multiple disciplines. As advancements in synthetic methodologies and material characterization techniques unfold, this compound is poised to play an even more significant role in shaping future technologies.
52089-10-8 ((3-bromophenyl)(phenyl)sulfane) Related Products
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
- 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
- 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
- 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
- 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
- 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
- 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
- 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)