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About This Item
Linear Formula:
C6H5CH(OH)CO2CH2C6H5
CAS Number:
Molecular Weight:
242.27
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
form
solid
optical activity
[α]25/D +55°, c = 1 in chloroform
mp
104-107 °C (lit.)
SMILES string
O[C@H](C(=O)OCc1ccccc1)c2ccccc2
InChI
1S/C15H14O3/c16-14(13-9-5-2-6-10-13)15(17)18-11-12-7-3-1-4-8-12/h1-10,14,16H,11H2/t14-/m0/s1
InChI key
JFKWZVQEMSKSBU-AWEZNQCLSA-N
Application
Benzyl (S)-(+)-mandelate can be used as a reactant to prepare:
- α-Hydroxy-N-(2-phenylethyl)benzenepropanamide by reacting with benzeneethanamine.
- Benzyl-2-fluoro-2-phenylacetate by deoxyfluorination of alcohols.
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
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Find documentation for the products that you have recently purchased in the Document Library.
Stereoselective Pseudomonas cepacia lipase mediated synthesis of α-hydroxyamides
Adamczyk M, et al.
Tetrahedron Asymmetry, 8(15), 2509-2512 (1997)
AlkylFluor: Deoxyfluorination of Alcohols.
Goldberg NW, et al.
Organic Letters, 18(23), 6102-6104 (2016)
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