All Photos(1)
Synonym(s):
(R)-2-Hydroxy-2-phenylacetophenone
Linear Formula:
C6H5CH(OH)COC6H5
CAS Number:
Molecular Weight:
212.24
MDL number:
UNSPSC Code:
12352115
PubChem Substance ID:
Recommended Products
Assay
98%
optical activity
[α]24/D −115°, c = 1.5 in acetone
optical purity
ee: 99% (HPLC)
mp
135-137 °C (lit.)
SMILES string
O[C@H](c1ccccc1)C(=O)c2ccccc2
InChI
1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H/t13-/m1/s1
InChI key
ISAOCJYIOMOJEB-CYBMUJFWSA-N
Application
(R)-(-)-Benzoin may be used in the preparation of (R)-2-hydroxy-1-phenylpropanone by reacting with benzaldehyde lyase (BAL) in the presence of acetaldehyde.
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Hung-Wei Tsui et al.
Journal of chromatography. A, 1637, 461796-461796 (2021-01-03)
The effect of solvents on the enantioselectivities of four structurally similar chiral solutes with a cellulose derivative-based chiral stationary phase, Chiralpak IB, were studied using acetone (AC), 2-propanol (IPA), and tert-butanol (TBA) separately as polar modifiers. The enantioselectivities α of
Rüdiger Ohs et al.
Biotechnology progress, 35(6), e2868-e2868 (2019-06-18)
The kinetic description of enzyme-catalyzed reactions is a core task in biotechnology and biochemical engineering. In particular, mechanistic kinetic models help from the discovery of the biocatalyst throughout its application. Chemo- or enantioselective enzyme reactions often undergo two alternative pathways
Rüdiger Ohs et al.
Biotechnology progress, 34(5), 1081-1092 (2018-06-10)
Thiamine diphosphate (ThDP)-dependent enzymes catalyze a broad range of reactions with excellent enantioselectivity. Among these reactions, carboligations of aldehydes are of particular interest since the products, chiral hydroxy ketones, are valuable building blocks in the pharmaceutical industry. However, the substrates
Chromatograms
application for HPLCapplication for HPLCOur team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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