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282693

Sigma-Aldrich

(S)-(+)-2-Phenylglycinol

98%

Synonym(s):

(S)-2-Amino-2-phenylethanol, L-(+)-α-Phenylglycinol

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About This Item

Linear Formula:
C6H5CH(NH2)CH2OH
CAS Number:
20989-17-7
Molecular Weight:
137.18
Beilstein/REAXYS Number:
3196190
MDL number:
MFCD00064404
UNSPSC Code:
12352209
PubChem Substance ID:
24857063
NACRES:
NA.22

Quality Level

200

assay

98%

form

solid

optical activity

[α]19/D +33°, c = 0.75 in 1 M HCl

optical purity

ee: 99% (GLC)

reaction suitability

reaction type: solution phase peptide synthesis

mp

75-78 °C (lit.)

application(s)

peptide synthesis

SMILES string

N[C@H](CO)c1ccccc1

InChI

1S/C8H11NO/c9-8(6-10)7-4-2-1-3-5-7/h1-5,8,10H,6,9H2/t8-/m1/s1

InChI key

IJXJGQCXFSSHNL-MRVPVSSYSA-N

Related Categories

Application

Used in a synthesis of chiral, unsymmetrical bisoxazolines.

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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D−(−)-α-Phenylglycine 99%

Sigma-Aldrich

P25485

D−(−)-α-Phenylglycine

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Jin Han et al.
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The present study describes our continuous effort to develop epidermal growth factor receptor (EGFR) inhibitors based on the 6-aryl-pyrrolo[2,3-d]pyrimidin-4-amine scaffold. The activity-ADME space has been evaluated by synthesizing 43 new structures, including four variations of the 4-amino group and 34

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