- 2-amino-4-bromophenol
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- $0.00 / 1kg
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2025-09-16
- CAS:40925-68-6
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1 ton
- 2-Amino-4-bromophenol
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- $0.00 / 25kg
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2025-05-12
- CAS:40925-68-6
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 2 MTs
- 2-Amino-4-bromophenol
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- $2.00 / 1KG
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2019-07-06
- CAS:40925-68-6
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: Customise
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| | 2-Amino-4-bromophenol Basic information |
| | 2-Amino-4-bromophenol Chemical Properties |
| Melting point | 135-140°C | | Boiling point | 282.8±25.0 °C(Predicted) | | density | 1.768±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | form | powder to crystal | | pka | 9.19±0.18(Predicted) | | color | White to Gray to Brown | | BRN | 3236448 | | InChI | InChI=1S/C6H6BrNO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,8H2 | | InChIKey | JHRIPENGTGSNPJ-UHFFFAOYSA-N | | SMILES | C1(O)=CC=C(Br)C=C1N | | CAS DataBase Reference | 40925-68-6(CAS DataBase Reference) |
| Hazard Codes | Xi,Xn | | Risk Statements | 20/21/22-36/37/38-42/43-22 | | Safety Statements | 26-36/37/39-36/37-22 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29222990 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral Eye Irrit. 2 Resp. Sens. 1 Skin Irrit. 2 Skin Sens. 1 STOT SE 3 |
| | 2-Amino-4-bromophenol Usage And Synthesis |
| Description | 2-Amino-4-bromophenol is a reactant for the preparation of (aryl)oxadiazolobenzoxazinones via Suzuki-Miyaura reaction, copper-catalyzed oxidative amination of benzoxazoles and related azoles via C-H and C-N bond activation synthesis of N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives as protein tyrosine phophatase 1B inhibitors,preparation of lipophilic deoxy-xylulose-phosphate reductoisomerase inhibitors,synthesis of benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphatase. | | Chemical Properties | White solid | | Uses | Reactant for:
- Preparation of (aryl)oxadiazolobenzoxazinones via Suzuki-Miyaura reaction
- Copper-catalyzed oxidative amination of benzoxazoles and related azoles via C-H and C-N bond activation
- Synthesis of N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives as protein tyrosine phophatase 1B inhibitors
- Preparation of lipophilic deoxy-xylulose-phosphate reductoisomerase inhibitors
- Synthesis of benzoxazole benzenesulfonamides as allosteric inhibitors of fructose-1,6-bisphosphatase
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| | 2-Amino-4-bromophenol Preparation Products And Raw materials |
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