Cas no 274-30-6 (1,3-Benzodithiole)
1,3-Benzodithiole is a heterocyclic organic compound featuring a benzene ring fused with a 1,3-dithiole moiety. This structure imparts unique electronic and coordination properties, making it valuable in materials science and organic synthesis. Its sulfur-rich framework enables applications in conductive polymers, charge-transfer complexes, and as a ligand in transition metal chemistry. The compound's rigid, planar geometry and electron-donating characteristics enhance its utility in designing redox-active materials and organic semiconductors. Additionally, 1,3-benzodithiole serves as a precursor for functionalized derivatives used in optoelectronic devices and catalysis. Its stability and reactivity under controlled conditions make it a versatile intermediate in advanced chemical research.
1,3-Benzodithiole structure
Product Name:1,3-Benzodithiole
1,3-Benzodithiole Chemical and Physical Properties
Names and Identifiers
-
- 1,3-Benzodithiole
- 1,2-(Methylenedithio)benzene
- 1,3-benzodithiolane
- 1.3-Benzodithiol
- Benzene,1,2-[methylenebis(thio)]
- benzo[1,3]dithiole
- 1,3-BENZODITHIOL
- 2H-1,3-benzodithiole
- FCH1115741
- CS-15724
- Benzo[d][1,3]dithiole
- SCHEMBL8630662
- starbld0009767
- 274-30-6
- D71935
- DTXSID50482211
- AKOS000279316
- SCHEMBL255965
- SY318806
- SCHEMBL7202298
- CS-0040606
- 1, 3-benzodithiole
- HCMLNPZTRYNCMA-UHFFFAOYSA-N
-
- Inchi： 1S/C7H6S2/c1-2-4-7-6(3-1)8-5-9-7/h1-4H,5H2
- InChI Key： HCMLNPZTRYNCMA-UHFFFAOYSA-N
- SMILES： S1CSC2C=CC=CC1=2
Computed Properties
- Exact Mass: 153.99100
- Monoisotopic Mass: 153.99109254g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 9
- Rotatable Bond Count: 0
- Complexity: 91.1
- 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: 2.8
- Topological Polar Surface Area: 50.6
Experimental Properties
- PSA: 50.60000
- LogP: 2.84190
1,3-Benzodithiole Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| ChemScence | CS-0040606-100mg |
1,3-Benzodithiole |
274-30-6 | 100mg |
$120.0 | 2022-04-27 | ||
| ChemScence | CS-0040606-250mg |
1,3-Benzodithiole |
274-30-6 | 250mg |
$200.0 | 2022-04-27 | ||
| ChemScence | CS-0040606-1g |
1,3-Benzodithiole |
274-30-6 | 1g |
$400.0 | 2022-04-27 | ||
| eNovation Chemicals LLC | Y1248168-100mg |
1,3-BENZODITHIOL |
274-30-6 | 95% | 100mg |
$190 | 2024-06-06 | |
| eNovation Chemicals LLC | Y1248168-250mg |
1,3-BENZODITHIOL |
274-30-6 | 95% | 250mg |
$255 | 2024-06-06 | |
| eNovation Chemicals LLC | Y1248168-1g |
1,3-BENZODITHIOL |
274-30-6 | 95% | 1g |
$475 | 2024-06-06 | |
| Aaron | AR00C5M8-100mg |
1,3-BENZODITHIOL |
274-30-6 | 95% | 100mg |
$125.00 | 2023-12-14 | |
| Aaron | AR00C5M8-250mg |
1,3-BENZODITHIOL |
274-30-6 | 95% | 250mg |
$208.00 | 2023-12-14 | |
| Aaron | AR00C5M8-1g |
1,3-BENZODITHIOL |
274-30-6 | 95% | 1g |
$416.00 | 2023-12-14 | |
| 1PlusChem | 1P00C5DW-100mg |
1,3-BENZODITHIOL |
274-30-6 | >98% | 100mg |
$195.00 | 2024-05-07 |
1,3-Benzodithiole Related Literature
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1. Synthesis, separation and absolute configuration assignment to enantiomers of 1,3-benzodithiole 1-oxide and 2-alkyl-1,3-benzodithiole 1-oxidesDerek R. Boyd,Narain D. Sharma,James H. Gorman,Robert Dunlop,John F. Malone,R. Austin S. McMordie,Alex F. Drake J. Chem. Soc. Perkin Trans. 1 1992 1105
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2. Dithiols. Part 29. Syntheses of cis- and trans-2-phenyliminoperhydro-1,3-benzodithioleRichard C. Forster,Leonard N. Owen J. Chem. Soc. Perkin Trans. 1 1978 1208
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3. Stereoselective reductase-catalysed deoxygenation of sulfoxides in aerobic and anaerobic bacteriaDerek R. Boyd,Narain D. Sharma,Alistair W. T. King,Steven D. Shepherd,Christopher C. R. Allen,Robert A. Holt,Heather R. Luckarift,Howard Dalton Org. Biomol. Chem. 2004 2 554
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4. Preparation, X-ray structures and unique redox reactions of novel 2,2′-(2,2-dimethylpropane-1,3-diylidene)bis(1,3-benzodithiole)-type electron donors fused with a naphthalene ringTakanori Suzuki,Tsuyoshi Yoshino,Masakazu Ohkita,Takashi Tsuji J. Chem. Soc. Perkin Trans. 1 2000 3417
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Hiroshi Nishimoto,Tomofumi Kadoya,Rikyu Miyake,Takeshi Oda,Jun-ichi Nishida,Kazuya Kubo,Hiroyuki Tajima,Takeshi Kawase,Jun-ichi Yamada CrystEngComm 2022 24 5562
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