Details
High quality purity >99% L-Phenylacetyl Carbinol 53439-91-1 for sale
- Molecular Formula: C9H10O2
- Molecular Weight: 150.177
- Boiling Point: 253.3±20.0 °C(Predicted)
- PKA: 12.33±0.20(Predicted)
- PSA： 37.30000
- Density: 1.119±0.06 g/cm3(Predicted)
- LogP: 1.30900
53439-91-1 Relevant articles
A One-Pot Two-Step Enzymatic Pathway for the Synthesis of Enantiomerically Enriched Vicinal Diols
Giovannini, Pier Paolo,Müller, Michel,Presini, Francesco,Baraldi, Serena,Ragno, Daniele,Di Carmine, Graziano,Jacoby, Christian,Bernacchia, Giovanni,Bortolini, Olga
, p. 973 - 978 (2021/02/01)
Enantiomerically enriched 1,2-diols are ...
Whole-Cell Biocatalysis in Seawater: New Halotolerant Yeast Strains for the Regio- and Stereoselectivity Reduction of 1-Phenylpropane-1,2-Dione in Saline-Rich Media
Andreu, Cecilia,del Olmo, Marcellí
, p. 1621 - 1628 (2020/03/05)
The application of green chemistry conce...
Synthesis of α-hydroxy ketones and vicinal (R, R)-diols by Bacillus clausii DSM 8716T butanediol dehydrogenase
Bongaerts, Johannes,Jablonski, Melanie,Kipp, Carina Ronja,Molinnus, Denise,Muschallik, Lukas,Pohl, Martina,Sch?ning, Michael J.,Selmer, Thorsten,Siegert, Petra,Wagner, Torsten
, p. 12206 - 12216 (2020/04/20)
α-hydroxy ketones (HK) and 1,2-diols are...
Immobilized chiral rhodium nanoparticles stabilized by chiral P-ligands as efficient catalysts for the enantioselective hydrogenation of 1-phenyl-1,2-propanedione
Ruiz, Doris,M?ki-Arvela, P?ivi,Aho, Atte,Chiment?o, Ricardo,Claver, Carmen,Godard, Cyril,Fierro, José L.G.,Murzin, Dmitry Yu.
, (2019/08/26)
This work reports the efficient synthesi...
53439-91-1 Process route
-
-
917-64-6
methyl magnesium iodide
-
-
120443-82-5
(R)-2-phenyl-2-(trimethylsiloxy)acetonitrile
-
-
1798-60-3
(R)-1-hydroxy-1-phenyl-2-propanone
-
-
53439-91-1
(S)-phenylacetylcarbinol
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
1.) ether, reflux, 2 h;
|
|
|
With
sulfuric acid;
Yield given. Multistep reaction. Yields of byproduct given;
1.) ether, reflux, 4 h; 2.) 0 deg C, 8 h;
|
-
-
43108-63-0
1-phenyl-2-trimethylsiloxy-1-propene
-
-
1798-60-3
(R)-1-hydroxy-1-phenyl-2-propanone
-
-
53439-91-1
(S)-phenylacetylcarbinol
| Conditions | Yield |
|---|---|
|
With
(+)-(2S,8aS)-(camphorylsulfonyl)oxaziridine; methyllithium;
Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
1.) HMPA, THF, 0 deg C, 1h; 2.) -78 deg C;
|
53439-91-1 Upstream products
-
917-64-6
methyl magnesium iodide
-
120443-82-5
(R)-2-phenyl-2-(trimethylsiloxy)acetonitrile
-
43108-63-0
1-phenyl-2-trimethylsiloxy-1-propene
-
103-79-7
1-phenyl-acetone
53439-91-1 Downstream products
-
405146-52-3
(1S,2R)-2-((R)-2-Hydroxy-2-phenyl-ethoxyamino)-1-phenyl-propan-1-ol
-
492-39-7
(1S,2S)-2-amino-1-phenylpropanol
-
37577-28-9
(1S,2R)-(+)-norphedrine
-
100-52-7
benzaldehyde
Related Products
-
befiradolCAS：208110-64-9
-
Tetrakis(p-broMophenyl)MethaneCAS：105309-59-9
-
SCH772984CAS：942183-80-4