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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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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