- 2-Bromodibenzothiophene
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- $0.00 / 1KG
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2024-04-18
- CAS:22439-61-8
- Min. Order: 10g
- Purity: 99.90%
- Supply Ability: 10TONS
- 2-Bromodibenzothiophene
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- $0.00 / 25KG
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2024-04-17
- CAS:22439-61-8
- Min. Order: 1KG
- Purity: ≥99%
- Supply Ability: 100mt/year
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| | 2-BROMODIBENZOTHIOPHENE Basic information |
| Product Name: | 2-BROMODIBENZOTHIOPHENE | | Synonyms: | 2-BROMODIBENZOTHIOPHENE;NSC 172586;2-BroModibenzothiophene/
2-BroModibenzothiophene;Dibenzothiophene,2-bromo-;2-DCDT-A;2-Bromdibenzothiophene;2-Bromodibenzothiophene >;2-BROMODIBENZOTHIOPHENE ISO 9001：2015 REACH | | CAS: | 22439-61-8 | | MF: | C12H7BrS | | MW: | 263.15 | | EINECS: | 1308068-626-2 | | Product Categories: | OLED | | Mol File: | 22439-61-8.mol |  |
| | 2-BROMODIBENZOTHIOPHENE Chemical Properties |
| Melting point | 250-252℃ | | Boiling point | 387℃ | | density | 1.611 | | Fp | 188℃ | | storage temp. | Sealed in dry,Room Temperature | | solubility | DMSO (Sparingly), Ethyl Acetate (Slightly) | | form | Solid | | color | White to Off-White | | Water Solubility | Slightly soluble in water. | | InChI | InChI=1S/C12H7BrS/c13-8-5-6-12-10(7-8)9-3-1-2-4-11(9)14-12/h1-7H | | InChIKey | IJICRIUYZZESMW-UHFFFAOYSA-N | | SMILES | C12=CC=C(Br)C=C1C1=CC=CC=C1S2 |
| Safety Statements | 24/25 | | HS Code | 29309090 |
| | 2-BROMODIBENZOTHIOPHENE Usage And Synthesis |
| Chemical Properties | White solid | | Uses | Used as intermediate for organic light-emitting diode(OLED) materials and pharmaceutical. | | Uses | 2-BROMODIBENZOTHIOPHENE can be used as an intermediate to synthesize organic semiconductor molecules. It is mainly used to synthesize devices used in OLED, OFET and OPV. It can also be used as a raw material and pharmaceutical intermediate in drug discovery and industrial production synthesis. For example, new N-substituted dibenzothiophene derivatives are synthesized by conjugation with primary or secondary amines[1-2]. | | References | [1] Alelaiwi S, et al. One-Pot Synthesis of Aminated Benzo-Fused Heterocycles and N-Substituted Dibenzothiophenes via Copper-Catalyzed Ullmann Type Reaction. ACS Omega, 2021; 6: 6009–6016.[2] Avila-Ortega A, et al. Living anionic polymerization of 2-vinyldibenzothiophene: Homopolymer and block copolymers with styrene. Journal of Polymer Science Part A: Polymer Chemistry, 2007; 45: 1993-2003. |
| | 2-BROMODIBENZOTHIOPHENE Preparation Products And Raw materials |
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