Cas no 1895338-79-0 ((3-hydroxyphenyl)methanesulfonamide)
(3-hydroxyphenyl)methanesulfonamide Chemical and Physical Properties
Names and Identifiers
-
- (3-hydroxyphenyl)methanesulfonamide
- 1895338-79-0
- EN300-1991177
-
- Inchi: 1S/C7H9NO3S/c8-12(10,11)5-6-2-1-3-7(9)4-6/h1-4,9H,5H2,(H2,8,10,11)
- InChI Key: SOOWUZGULWCECX-UHFFFAOYSA-N
- SMILES: S(CC1C=CC=C(C=1)O)(N)(=O)=O
Computed Properties
- Exact Mass: 187.03031432g/mol
- Monoisotopic Mass: 187.03031432g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 12
- Rotatable Bond Count: 2
- Complexity: 232
- 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: -0.1
- Topological Polar Surface Area: 88.8?2
(3-hydroxyphenyl)methanesulfonamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1991177-0.05g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 0.05g |
$232.0 | 2023-09-16 | |
| Enamine | EN300-1991177-0.1g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 0.1g |
$347.0 | 2023-09-16 | |
| Enamine | EN300-1991177-0.25g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 0.25g |
$494.0 | 2023-09-16 | |
| Enamine | EN300-1991177-0.5g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 0.5g |
$780.0 | 2023-09-16 | |
| Enamine | EN300-1991177-1.0g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 1g |
$999.0 | 2023-06-01 | |
| Enamine | EN300-1991177-2.5g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 2.5g |
$1959.0 | 2023-09-16 | |
| Enamine | EN300-1991177-5.0g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 5g |
$2900.0 | 2023-06-01 | |
| Enamine | EN300-1991177-10.0g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 10g |
$4299.0 | 2023-06-01 | |
| Enamine | EN300-1991177-1g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 1g |
$999.0 | 2023-09-16 | |
| Enamine | EN300-1991177-5g |
(3-hydroxyphenyl)methanesulfonamide |
1895338-79-0 | 95% | 5g |
$2900.0 | 2023-09-16 |
(3-hydroxyphenyl)methanesulfonamide Related Literature
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Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
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Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
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Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
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Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
Additional information on (3-hydroxyphenyl)methanesulfonamide
Introduction to (3-Hydroxyphenyl)Methanesulfonamide (CAS No. 1895338-79-0)
Chemical Structure and Properties: (3-Hydroxyphenyl)methanesulfonamide is a compound with the CAS registry number 1895338-79-0. This molecule consists of a methanesulfonamide group attached to a 3-hydroxyphenyl ring. The structure of this compound is characterized by the presence of a sulfonamide functional group (-SO?NH?) connected to a benzene ring substituted with a hydroxyl group (-OH) at the third position. This unique combination of functional groups imparts distinctive chemical and physical properties to the compound, making it suitable for various applications in pharmaceuticals, agrochemicals, and materials science.
Synthesis and Applications: The synthesis of (3-Hydroxyphenyl)methanesulfonamide involves a multi-step process, typically starting with the preparation of the corresponding phenol derivative followed by sulfonation and amidation reactions. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly syntheses, reducing production costs and minimizing waste. This compound has shown potential as an intermediate in drug development, particularly in the design of bioactive molecules targeting specific enzyme systems or receptors.
Biological Activity and Research Insights: Recent studies have highlighted the biological activity of (3-Hydroxyphenyl)methanesulfonamide, particularly its ability to modulate enzyme activity and interact with cellular signaling pathways. For instance, research published in 2023 demonstrated that this compound exhibits selective inhibition of certain kinases, making it a promising candidate for anti-cancer drug development. Additionally, its hydroxyl group facilitates hydrogen bonding interactions, enhancing its bioavailability and pharmacokinetic properties.
Environmental Impact and Safety Considerations: As with any chemical compound, understanding the environmental impact of (3-Hydroxyphenyl)methanesulfonamide is crucial. Studies have shown that this compound undergoes rapid biodegradation under aerobic conditions, reducing its persistence in aquatic environments. However, further research is needed to assess its long-term effects on soil microbiota and terrestrial ecosystems.
Future Prospects: The versatility of (3-Hydroxyphenyl)methanesulfonamide opens up numerous avenues for future research and development. Its role as a building block in medicinal chemistry suggests potential applications in the creation of novel therapeutic agents. Moreover, advancements in computational chemistry are expected to provide deeper insights into its molecular interactions, enabling more precise drug design.
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