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309974

Sigma-Aldrich

Ethyl (S)-(+)-mandelate

99%, optical purity ee: 99% (GLC)

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About This Item

Linear Formula:
C6H5CH(OH)CO2C2H5
CAS Number:
13704-09-1
Molecular Weight:
180.20
MDL number:
MFCD00064249
UNSPSC Code:
12352108
PubChem Substance ID:
24858761
NACRES:
NA.22

assay

99%

form

solid

optical activity

[α]21/D +134°, c = 3 in chloroform

optical purity

ee: 99% (GLC)

bp

106-107 °C/4 mmHg (lit.)

mp

32-34 °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-/m0/s1

InChI key

SAXHIDRUJXPDOD-VIFPVBQESA-N

Application

Ethyl (S)-(+)-mandelate can be used as a starting material for the preparation of N-benzyl 2-phenylacetamide derivatives, which are known as potent anticonvulsant agents.[1]

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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Certificates of Analysis (COA)

Lot/Batch Number
MKBV9092V
MKBB3804
12928DW
01425CD
12917TZ

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The anticonvulsant activities of functionalized N-benzyl 2-acetamidoacetamides. The importance of the 2-acetamido substituent
Choi D, et al.
Bioorganic & Medicinal Chemistry, 4(12), 2105-2114 (1996)
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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