2-Hydroxybenzophenone manufacturers
- 2-Hydroxybenzophenone
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- $1.00 / 1KG
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2019-12-20
- CAS:117-99-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: KG/T
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| | 2-Hydroxybenzophenone Basic information |
| | 2-Hydroxybenzophenone Chemical Properties |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-37/39-36 | | WGK Germany | 3 | | TSCA | TSCA listed | | HazardClass | IRRITANT | | HS Code | 29145000 | | Storage Class | 10 - Combustible liquids |
| | 2-Hydroxybenzophenone Usage And Synthesis |
| Chemical Properties | yellow crystalline powder | | Uses | UV absorber in plastics. | | Uses | 2-Hydroxybenzophenone was used to quantify the metabolites of unmethylated extracts from the supernatants of Pseudomonas acidovorans cultures grown on 1,1-diphenylethylene. | | Application | 2-Hydroxybenzophenone was used to quantify the metabolites of unmethylated extracts from the supernatants of Pseudomonas acidovorans cultures grown on 1,1-diphenylethylene.
2-Hydroxybenzophenone forms copolymer 2-hydroxy, 3-allyl, 4,4′-dimethoxybenzophenone with methyl methacrylate.
It forms photostabilizer compounds with 2,2,6,6-tetramethylpiperidine under phase transfer catalysis conditions.
It reacts with 3-aminophenyl boronic acid to form macrocyclic boronates. | | Preparation | Preparation by Friedel–Crafts acylation of benzene in the presence of aluminium chloride,
with 2-hydroxybenzoyl chloride (salicylic acid chloride), (52%), (39%), at temperature <60°;
with o-anisoyl chloride. Demethylation occurred during the Friedel–Crafts acylation, especially in the presence of ferric chloride at 130–140°;
with 2-ethoxybenzoyl chloride in a boiling water bath (42%). | | Synthesis Reference(s) | Journal of the American Chemical Society, 76, p. 5469, 1954 DOI: 10.1021/ja01650a062
The Journal of Organic Chemistry, 32, p. 3844, 1967 DOI: 10.1021/jo01287a027 | | General Description | - 2-Hydroxybenzophenone forms copolymer 2-hydroxy, 3-allyl, 4,4′-dimethoxybenzophenone with methyl methacrylate.
- It forms photostabilizer compounds with 2,2,6,6-tetramethylpiperidine under phase transfer catalysis conditions.
- It reacts with 3-aminophenyl boronic acid to form macrocyclic boronates.
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| | 2-Hydroxybenzophenone Preparation Products And Raw materials |
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