- 3-Bromobenzophenone
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- $1.10
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2026-08-20
- CAS:1016-77-9
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons Min
- 3-Bromobenzophenone
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-
2026-06-30
- CAS:1016-77-9
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1000kg
- 3-Bromobenzophenone
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- $9.00
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2026-05-28
- CAS:1016-77-9
- Min. Order: 1KG
- Purity: 99.9
- Supply Ability: 1 ton
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| | 3-Bromobenzophenone Basic information |
| | 3-Bromobenzophenone Chemical Properties |
| Melting point | 74.5-77.5 °C(lit.) | | Boiling point | 347.5°C (rough estimate) | | density | 1.4245 (rough estimate) | | refractive index | 1.5130 (estimate) | | storage temp. | Inert atmosphere,Room Temperature | | Appearance | White to light yellow Solid | | InChI | InChI=1S/C13H9BrO/c14-12-8-4-7-11(9-12)13(15)10-5-2-1-3-6-10/h1-9H | | InChIKey | XNUMUNIJQMSNNN-UHFFFAOYSA-N | | SMILES | C(C1=CC=CC(Br)=C1)(C1=CC=CC=C1)=O | | CAS DataBase Reference | 1016-77-9(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 22-24/25-37/39-26 | | WGK Germany | 3 | | HS Code | 29147000 | | Storage Class | 11 - Combustible Solids |
| | 3-Bromobenzophenone Usage And Synthesis |
| Chemical Properties | Off-white to beige-yellowish or orange powder | | Uses | 3-Bromobenzophenone reacts with diphenylmethane to yield the bromo-TPE intermediate mTPE-Br, which serves as a building block for tetraphenylethylene-based derivatives[2]. | | Synthesis | 3-Bromobenzophenone can be prepared by a palladium-catalyzed Suzuki reaction between bromobenzoyl chlorides and boronic acids, serving as a key synthetic intermediate for ketoprofen[1]. It is also obtained from the reaction of 1,3-dibromobenzene with benzoyl chloride[2]. Alternatively, Suzuki coupling of 3-bromobenzoyl chloride with phenylboronic acid affords 3-bromobenzophenone in 64% yield[1]. | | References |
[1]do Amaral e Silva, N. A., & de Luna Martins, D. (2023). Suzuki–Miyaura Cross-Coupling for the Synthesis of Key Intermediates of Ketoprofen and Bifonazole Analogues. 27th International Electronic Conference on Synthetic Organic Chemistry, 105. https://doi.org/10.3390/ecsoc-27-16068
[2]Huang, J., Sun, N., Dong, Y., Tang, R., Lu, P., Cai, P., Li, Q., Ma, D., Qin, J., & Li, Z. (2012). Similar or Totally Different: The Control of Conjugation Degree through Minor Structural Modifications, and Deep‐Blue Aggregation‐Induced Emission Luminogens for Non‐Doped OLEDs. Advanced Functional Materials, 23(18), 2329–2337. https://doi.org/10.1002/adfm.201202639
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| | 3-Bromobenzophenone Preparation Products And Raw materials |
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