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309982

Ethyl (R)-(−)-mandelate

Name: Ethyl (<I>R</I>)-(−)-mandelate
Brand: ALDRICH

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

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About This Item

Linear Formula:

C₆H₅CH(OH)CO₂C₂H₅

CAS Number:

10606-72-1

Molecular Weight:

180.20

MDL number:

MFCD00064248

UNSPSC Code:

12352108

PubChem Substance ID:

24858762

NACRES:

NA.22

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.)

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Esters of mandelic acid as substrates for (S)-mandelate dehydrogenase from Pseudomonas putida: implications for the reaction mechanism.

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

Catalysis of the hydrolysis of ethyl mandelate and esterification of alpha-bromopropionic acid by lipase in microemulsions.

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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