- 2,5-Dibromothiazole
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- $0.00 / 25KG
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2025-08-08
- CAS:4175-78-4
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 50000KG/month
- 2,5-Dibromothiazole
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- $30.00 / 1KG
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2025-06-27
- CAS:4175-78-4
- Min. Order: 50KG
- Purity: 99%
- Supply Ability: 500000kg
- 2,5-DIBROMOTHIAZOLE
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- $35.00 / 1kg
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2024-04-20
- CAS:4175-78-4
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | 2,5-DIBROMOTHIAZOLE Basic information |
| Product Name: | 2,5-DIBROMOTHIAZOLE | | Synonyms: | 2,5-Dibromo-1,3-thiazole;2,5-DIBROMOTHIAZOLE;2,5-DIBROMOTHIAZOLE 95%;2,5-Dibromothiazole,97%;Thiazole, 2,5-dibroMo-;NSC 222407;2,5-Dibormothiazole;DibromoThiazole | | CAS: | 4175-78-4 | | MF: | C3HBr2NS | | MW: | 242.92 | | EINECS: | 628-983-7 | | Product Categories: | Building Blocks;C3 to C7;Chemical Synthesis;Halogenated Heterocycles;Heterocyclic Building Blocks;alkyl bromide;Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;ThiazolesHeterocyclic Building Blocks;Heterocyclic Compounds;Thiazoles;Sulphur Derivatives | | Mol File: | 4175-78-4.mol |  |
| | 2,5-DIBROMOTHIAZOLE Chemical Properties |
| Melting point | 45-49 °C (lit.) | | Boiling point | 242.8±13.0 °C(Predicted) | | density | 2.324±0.06 g/cm3(Predicted) | | Fp | 110 °C | | storage temp. | Inert atmosphere,Store in freezer, under -20°C | | solubility | soluble in Methanol | | pka | -0.88±0.10(Predicted) | | form | Crystalline Powder | | color | White to brown | | InChI | InChI=1S/C3HBr2NS/c4-2-1-6-3(5)7-2/h1H | | InChIKey | XIBIQFJKUZZLLX-UHFFFAOYSA-N | | SMILES | S1C(Br)=CN=C1Br | | CAS DataBase Reference | 4175-78-4(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | Hazard Note | Harmful | | HS Code | 29341000 |
| | 2,5-DIBROMOTHIAZOLE Usage And Synthesis |
| Chemical Properties | White to brown crystalline powder | | Uses | Used as a building block in material science.1,2 | | Uses | 2,5-Dibromothiazole is used in the preparation of arylthiazolylpiperidine derivatives and analogs for use as survival motor neuron (SMN) protein production modulators. | | Synthesis | 2-Amino-5-bromothiazole (5.5 g, 30.72 mmol) was used as starting material and dissolved in acetonitrile (50 mL). Copper (II) bromide (3.43 g, 15.36 mmol) and isoamyl nitrite (4.9 mL, 36.87 mmol) were added sequentially. The reaction mixture was heated at 60 °C for 4 h with stirring. After completion of the reaction, the volatile solvent was removed by rotary evaporator. The residue was diluted with distilled water (50 mL) and subsequently extracted with ethyl acetate (25 mL x 2). The organic phases were combined, washed with saturated saline (50 mL) and dried over anhydrous sodium sulfate. The organic phase was concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography (60-120 mesh, eluent 10% ethyl acetate in hexane solution) to afford the target compound 2,5-dibromothiazole (5.05 g, yield 68%) as a yellow liquid. m/z 243.6 [M+2] by LCMS. | | References | [1] Patent: WO2015/88045, 2015, A1. Location in patent: Paragraph 0260
[2] Patent: US2017/8885, 2017, A1. Location in patent: Paragraph 0672-0673
[3] Bulletin de la Societe Chimique de France, 1962, p. 2075 - 2078
[4] Journal of Organic Chemistry, 2017, vol. 82, # 11, p. 5947 - 5951 |
| | 2,5-DIBROMOTHIAZOLE Preparation Products And Raw materials |
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