1-Hydroxy-3-phenyl-2-propanone - CAS 4982-08-5
Catalog: |
BB026829 |
Product Name: |
1-Hydroxy-3-phenyl-2-propanone |
CAS: |
4982-08-5 |
Synonyms: |
1-hydroxy-3-phenyl-2-propanone; 1-hydroxy-3-phenylpropan-2-one |
IUPAC Name: | 1-hydroxy-3-phenylpropan-2-one |
Description: | 1-Hydroxy-3-phenyl-2-propanone (CAS# 4982-08-5 ) is a useful research chemical. |
Molecular Weight: | 150.17 |
Molecular Formula: | C9H10O2 |
Canonical SMILES: | C1=CC=C(C=C1)CC(=O)CO |
InChI: | InChI=1S/C9H10O2/c10-7-9(11)6-8-4-2-1-3-5-8/h1-5,10H,6-7H2 |
InChI Key: | QLCZRWKIQPLYFS-UHFFFAOYSA-N |
MDL: | MFCD11036274 |
LogP: | 0.79050 |
Publication Number | Title | Priority Date |
CN-112852771-A | Enzymatic synthesis of chiral amino alcohol compounds | 20200417 |
US-10869845-B1 | Ephedrine compositions and methods | 20200122 |
CN-110628739-A | Amine dehydrogenase mutant and application thereof in synthesis of chiral amine and amino alcohol | 20190814 |
CN-110628739-B | Amine dehydrogenase mutant and application thereof in synthesis of chiral amine and amino alcohol | 20190814 |
WO-2020129087-A1 | NOVEL PROCESS FOR THE PREPARATION OF R-PHENYLACETYLCARBINOL AND β-AMINOALCOHOLS | 20181222 |
PMID | Publication Date | Title | Journal |
22727117 | 20120901 | Benzaldehyde is a precursor of phenylpropylamino alkaloids as revealed by targeted metabolic profiling and comparative biochemical analyses in Ephedra spp | Phytochemistry |
21341803 | 20110316 | Conversion of pyruvate decarboxylase into an enantioselective carboligase with biosynthetic potential | Journal of the American Chemical Society |
20878540 | 20110101 | The effects of polymer phase ratio and feeding strategy on solid-liquid TPPBs for the production of L-phenylacetylcarbinol from benzaldehyde using Candida utilis | Biotechnology letters |
20552670 | 20101101 | Application of solid-liquid TPPBs to the production of L-phenylacetylcarbinol from benzaldehyde using Candida utilis | Biotechnology and bioengineering |
19562522 | 20100301 | A closed concept of extractive whole cell microbial transformation of benzaldehyde into L-phenylacetylcarbinol by Saccharomyces cerevisiae in novel polyethylene-glycol-induced cloud-point system | Applied biochemistry and biotechnology |
Complexity: | 126 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 150.068079557 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 150.068079557 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 37.3 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.8 |
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