Cas no 4210-03-1 (Benzene, 1,3-dichloro-2-(methylthio)-)
Benzene, 1,3-dichloro-2-(methylthio)- Chemical and Physical Properties
Names and Identifiers
-
- Benzene, 1,3-dichloro-2-(methylthio)-
- 2,6-DICHLOROTHIOANISOLE
- 1,3-DICHLORO-2-(METHYLSULFANYL)BENZENE
- (2,6-Dichlorophenyl)(methyl)sulfane
- 4210-03-1
- MFCD03789170
- AKOS006241107
- SCHEMBL5594805
- 1,3-dichloro-2-methylsulfanylbenzene
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- MDL： MFCD03789170
- Inchi： 1S/C7H6Cl2S/c1-10-7-5(8)3-2-4-6(7)9/h2-4H,1H3
- InChI Key： RRXLOEAZYVLTJP-UHFFFAOYSA-N
- SMILES： ClC1C=CC=C(C=1SC)Cl
Computed Properties
- Exact Mass: 191.95688
- Monoisotopic Mass: 191.957
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 10
- Rotatable Bond Count: 1
- Complexity: 97.8
- 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: 3.7
- Topological Polar Surface Area: 25.3?2
Experimental Properties
- PSA: 0
Benzene, 1,3-dichloro-2-(methylthio)- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 019346-5g |
2,6-Dichlorothioanisole |
4210-03-1 | 98% | 5g |
￡34.00 | 2022-03-01 | |
| Fluorochem | 019346-1g |
2,6-Dichlorothioanisole |
4210-03-1 | 98% | 1g |
￡11.00 | 2022-03-01 | |
| abcr | AB524007-1 g |
2,6-Dichlorothioanisole, 95%; . |
4210-03-1 | 95% | 1g |
€49.60 | 2023-04-17 | |
| abcr | AB524007-5 g |
2,6-Dichlorothioanisole, 95%; . |
4210-03-1 | 95% | 5g |
€90.60 | 2023-04-17 | |
| abcr | AB524007-25g |
2,6-Dichlorothioanisole, 95%; . |
4210-03-1 | 95% | 25g |
€1144.70 | 2025-04-18 | |
| eNovation Chemicals LLC | Y1258902-250mg |
2,6-Dichlorothioanisole |
4210-03-1 | 97% | 250mg |
$120 | 2025-02-20 | |
| eNovation Chemicals LLC | Y1258902-100mg |
2,6-Dichlorothioanisole |
4210-03-1 | 97% | 100mg |
$105 | 2025-02-20 | |
| eNovation Chemicals LLC | Y1258902-500mg |
2,6-Dichlorothioanisole |
4210-03-1 | 97% | 500mg |
$130 | 2025-02-20 | |
| eNovation Chemicals LLC | Y1258902-1g |
2,6-Dichlorothioanisole |
4210-03-1 | 97% | 1g |
$155 | 2025-02-20 | |
| eNovation Chemicals LLC | Y1258902-10g |
2,6-Dichlorothioanisole |
4210-03-1 | 97% | 10g |
$530 | 2025-02-20 |
Benzene, 1,3-dichloro-2-(methylthio)- Related Literature
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
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Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
Additional information on Benzene, 1,3-dichloro-2-(methylthio)-
Introduction to CAS No. 4210-03-1: Benzene, 1,3-dichloro-2-(methylthio)-
CAS No. 4210-03-1, commonly referred to as Benzene, 1,3-dichloro-2-(methylthio)-, is a significant compound in the field of organic chemistry. This compound is characterized by its unique structure and properties, making it a subject of interest in various research and industrial applications.
The chemical structure of Benzene, 1,3-dichloro-2-(methylthio)- consists of a benzene ring with two chlorine atoms at positions 1 and 3 and a methylthio group (-SMe) at position 2. This arrangement imparts distinct electronic and steric properties to the molecule. The methylthio group acts as an electron-donating substituent through resonance effects, which can influence the reactivity of the benzene ring in various chemical reactions.
Recent studies have highlighted the potential of this compound in the synthesis of advanced materials and pharmaceuticals. For instance, researchers have explored its role as an intermediate in the production of biologically active compounds with potential applications in drug discovery. The ability of Benzene, 1,3-dichloro-2-(methylthio)- to undergo nucleophilic aromatic substitution reactions has been particularly valuable in constructing complex molecular architectures.
In terms of physical properties, this compound exhibits a melting point of approximately -5°C and a boiling point around 85°C under standard conditions. Its solubility in organic solvents such as dichloromethane and diethyl ether is relatively high compared to its solubility in water. These characteristics make it suitable for use in various organic synthesis protocols where controlled solubility is essential.
The synthesis of CAS No. 4210-03-1 typically involves chlorination reactions on substituted benzene derivatives. Recent advancements in catalytic methods have enabled more efficient and selective syntheses, reducing the environmental footprint associated with traditional manufacturing processes. These improvements align with current trends toward sustainable chemistry practices.
From an environmental perspective, understanding the fate and transport of Benzene, 1,3-dichloro-2-(methylthio)- in natural systems is crucial for assessing its potential impact on ecosystems. Studies have shown that this compound undergoes biodegradation under aerobic conditions; however, its persistence in certain environments remains a topic of ongoing research.
In conclusion, CAS No. 4210-03-1, or Benzene, 1,3-dichloro-2-(methylthio)-, stands out as a versatile compound with diverse applications across multiple disciplines. Its unique chemical properties continue to drive innovative research efforts aimed at harnessing its potential while ensuring environmentally responsible practices.
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