Cas no 4850-71-9 ((R)-(Methylsulfinyl)benzene)
(R)-(Methylsulfinyl)benzene Chemical and Physical Properties
Names and Identifiers
-
- [(R)-methylsulfinyl]benzene
- SB47809
- (R)-(methylsulphinyl)benzene
- CHEBI:134282
- (r)-methyl phenyl sulfoxide
- (R)-thioanisole S-oxide
- (R)-MPSO
- 4850-71-9
- SCHEMBL4801663
- (R)-(Methylsulfinyl)benzene
- (R)-Methanesulfinyl-benzene
- (S)-(Methylsulfinyl)benzene
- (R)-phenyl methyl sulfoxide
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- Inchi: 1S/C7H8OS/c1-9(8)7-5-3-2-4-6-7/h2-6H,1H3/t9-/m1/s1
- InChI Key: JXTGICXCHWMCPM-SECBINFHSA-N
- SMILES: [S@@](C)(C1C=CC=CC=1)=O
Computed Properties
- Exact Mass: 140.02958605Da
- Monoisotopic Mass: 140.02958605Da
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 105
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 1
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 0.6
- Topological Polar Surface Area: 36.3?2
Experimental Properties
- PSA: 36.28000
- LogP: 2.28970
(R)-(Methylsulfinyl)benzene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Ambeed | A856889-100mg |
(R)-(Methylsulfinyl)benzene |
4850-71-9 | 97% 98%ee | 100mg |
$154.0 | 2025-04-19 | |
| Ambeed | A856889-250mg |
(R)-(Methylsulfinyl)benzene |
4850-71-9 | 97% 98%ee | 250mg |
$248.0 | 2025-04-19 | |
| Ambeed | A856889-1g |
(R)-(Methylsulfinyl)benzene |
4850-71-9 | 97% 98%ee | 1g |
$650.0 | 2025-04-19 | |
| Ambeed | A856889-5g |
(R)-(Methylsulfinyl)benzene |
4850-71-9 | 97% 98%ee | 5g |
$2284.0 | 2025-04-19 | |
| SHANG HAI SHAO YUAN SHI JI Co., Ltd. | A01_9372586-100mg |
(R)-Methyl Phenyl Sulfoxide, 98% |
4850-71-9 | 98% | 100mg |
¥1413.00 | 2025-04-14 |
(R)-(Methylsulfinyl)benzene Suppliers
(R)-(Methylsulfinyl)benzene Related Literature
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Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
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Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812
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Ni-Na Sun,Fengli Qu,Xiaobing Zhang,Shufang Zhang,Jinmao You Analyst, 2015,140, 1827-1831
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Govind Reddy Mol. Syst. Des. Eng., 2021,6, 779-789
Additional information on (R)-(Methylsulfinyl)benzene
Introduction to (R)-(Methylsulfinyl)benzene (CAS No. 4850-71-9)
(R)-(Methylsulfinyl)benzene, with the chemical formula C?H?OS, is a significant compound in the field of pharmaceutical and chemical research. Its CAS number, 4850-71-9, uniquely identifies it in scientific literature and databases. This compound has garnered attention due to its unique structural properties and potential applications in various chemical synthesis processes.
The< strong>methylsulfinyl group attached to the benzene ring introduces a distinct electronic and steric environment, making (R)-(Methylsulfinyl)benzene a versatile intermediate in organic synthesis. The chirality imparted by the (R) configuration further enhances its utility in pharmaceutical applications, where enantiomeric purity is often critical.
In recent years, there has been growing interest in the development of novel therapeutic agents derived from sulfoxide-containing compounds. (R)-(Methylsulfinyl)benzene has emerged as a valuable building block in this context. Its ability to participate in various chemical reactions, such as nucleophilic substitution and metal-catalyzed coupling reactions, makes it a preferred choice for synthetic chemists.
One of the most compelling aspects of (R)-(Methylsulfinyl)benzene is its role in the synthesis of biologically active molecules. Researchers have leveraged its structural features to develop new drugs targeting various diseases. For instance, sulfoxides have been shown to exhibit anti-inflammatory, anti-cancer, and antimicrobial properties. The (R)-configuration of this compound ensures that any derivatives maintain high enantiomeric purity, which is crucial for achieving optimal pharmacological activity.
The pharmaceutical industry has been particularly interested in exploring the potential of (R)-(Methylsulfinyl)benzene as a precursor for drug development. Its incorporation into complex molecular frameworks allows for the creation of novel scaffolds with improved pharmacokinetic profiles. This has led to several preclinical studies investigating its derivatives as potential treatments for conditions ranging from neurological disorders to chronic inflammatory diseases.
Furthermore, the synthetic versatility of (R)-(Methylsulfinyl)benzene has opened up new avenues in materials science. Researchers have utilized this compound to develop advanced polymers and coatings with enhanced durability and functionality. The presence of the sulfoxide group imparts unique electronic properties, making it suitable for applications in conductive materials and sensors.
The production and handling of (R)-(Methylsulfinyl)benzene require stringent quality control measures to ensure consistency and purity. Modern synthetic techniques, such as chiral resolution and catalytic asymmetric synthesis, have enabled the efficient production of this compound on an industrial scale. These advancements have not only improved yield but also reduced costs, making it more accessible for research and commercial applications.
In conclusion, (R)-(Methylsulfinyl)benzene (CAS No. 4850-71-9) is a multifaceted compound with significant implications in pharmaceutical chemistry and materials science. Its unique structural features and synthetic versatility make it a valuable asset in the development of new drugs and advanced materials. As research continues to uncover new applications for this compound, its importance is likely to grow further, solidifying its role as a cornerstone in modern chemical innovation.
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