309982
Ethyl (R)-(−)-mandelate
99%, optical purity ee: 99% (GLC)
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About This Item
Linear Formula:
C6H5CH(OH)CO2C2H5
CAS Number:
Molecular Weight:
180.20
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
99%
form
solid
optical activity
[α]21/D −134°, c = 3 in chloroform
optical purity
ee: 99% (GLC)
bp
103-105 °C/2 mmHg (lit.)
mp
33-34 °C (lit.)
functional group
ester
hydroxyl
phenyl
SMILES string
CCOC(=O)[C@H](O)c1ccccc1
InChI
1S/C10H12O3/c1-2-13-10(12)9(11)8-6-4-3-5-7-8/h3-7,9,11H,2H2,1H3/t9-/m1/s1
InChI key
SAXHIDRUJXPDOD-SECBINFHSA-N
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Asteriani R Dewanti et al.
Biochemistry, 43(7), 1883-1890 (2004-02-18)
(S)-Mandelate dehydrogenase (MDH) from Pseudomonas putida is a flavin mononucleotide (FMN)-dependent enzyme that oxidizes (S)-mandelate to benzoylformate. In this work, we show that the ethyl and methyl esters of (S)-mandelic acid are substrates for MDH. Although the binding affinity of
H Xiao et al.
Chinese journal of biotechnology, 9(1), 33-39 (1993-01-01)
Candida cyclindracea lipase (CCL) was added to "sodium dodecyl sulfonate (AS)/n-butanol/n-octane/n-octane" water-in-oil microemulsion to catalyze the hydrolysis of ethyl mandelate and the esterification of alpha-bromopropionic acid with n-butanol, respectively. The catalytic activity of CCL in the above microemulsions was higher
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