description: 3-Phenyl-1-butanol undergoes biotransformation to aldehydes by oxidation in the presence of Gluconobacteroxydans DSM 2343. It undergoes enantioselective transesterification reaction with vinyl acetate catalyzed by lipase isolated from Pseudomonas cepacia. application: 3-Phenyl-1-butanol is a reactant with primary alcohol functional group which is oxidized to aldehyde using the nanoparticle-ferrite-palladium catalyst.
All
Chemical Reagents
Biomedicine
Organic raw materials
Inorganic chemical industry
intermediate
Agricultural chemicals
Auxiliaries and catalysts
Fragrances and Flavors
Dyes and Pigments
Daily chemical industry
3-Phenyl-1-butanol
Dangerous GoodsCAS number:2722-36-3 molecular formula:C10H14O
overview
compound introduction
Specs
| Chinese alias | - | ||
| English alias | 3-Phenyl-1-butanol | 3-Phenylbutan-1-ol | 2722-36-3 | Benzenepropanol, .gamma.-methyl- | 3-phenyl butanol | 3-phenyl-butanol | EINECS 220-335-8 | AI3-11558 | Benzenepropanol,g-methyl- | (+)-3-phenyl-l-butanol | (+)-3-phenyl-1-butanol | SCHEMBL81404 | 3-Ph | ||
| CAS number | 2722-36-3 | molecular formula | C10H14O |
| molecular weight | 150.22 g/mol | Exact mass | ≥96% |
| PSA | 20.200 Ų | logp | 2.200 |
numbering system
No numbering system information yet
physicochemical properties
No physical and chemical property information yet
Safety information
WGK Germany:
3
Personal protective equipment:
Eyeshields, Gloves
Production methods and uses
No production method and use information yet
Related
upstream information
No upstream information yet
downstream information
No downstream information yet
MSDS
Found 1 shareMSDS
2722-36-3 | 3-Phenyl-1-butanol.pdf





