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459941
(R)-(−)-Benzoin
98%
Synonym(e):
(R)-2-Hydroxy-2-phenylacetophenon
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About This Item
Empfohlene Produkte
Assay
98%
Optische Aktivität
[α]24/D −115°, c = 1.5 in acetone
Optische Reinheit
ee: 99% (HPLC)
mp (Schmelzpunkt)
135-137 °C (lit.)
Funktionelle Gruppe
hydroxyl
ketone
phenyl
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
InChIKey
ISAOCJYIOMOJEB-CYBMUJFWSA-N
Anwendung
(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.
Anwendung
Produkt-Nr.
Beschreibung
Preisangaben
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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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
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
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
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