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Substance
ID:328786
Structure
Similarity
Functional Group
Text
ID:68506
(-)-N-Boc-D-α-phenylglycinol
Sigma Aldrich
ID: 429813
Names and Identifiers
IUPAC Traditional name
tert-butyl N-[(1R)-2-hydroxy-1-phenylethyl]carbamate
IUPAC name
tert-butyl N-[(1R)-2-hydroxy-1-phenylethyl]carbamate
Synonyms
(-)-N-Boc-D-α-phenylglycinol
(R)-N-叔丁氧羰基-2-苯甘氨醇
(R)-(-)-2-(Boc-amino)-2-phenylethanol
(R)-(-)-2-(Boc-氨基)-2-苯乙醇
Registration numbers
MDL Number
MFCD00274205
CAS Number
102089-74-7
Beilstein Number
4688248
PubChem SID
24866892
Properties
Safety Information
German water hazard class
3
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
MSDS Link
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Product Information
Purity
99%
Optical Purity
ee: 99% (GLC)
Linear Formula
(CH3)3CO2CNHCH(C6H5)CH2OH
Physical Property
Melting Point
137-139 °C(lit.)
Optical Rotation
[α]19/D -38°, c = 1 in chloroform
Molecule Details
Application
Used for the synthesis of homochiral N-protected β-amino sulfoxides1 and α-amino acids.2 Chiral synthon, which undergoes heterocyclizations.3 Precursor to chiral oxazolidinones.4
Packaging
1 g in glass bottle
Molecular Spectra
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References
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