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282693

(S)-(+)-2-Phenylglycinol

98%, for peptide synthesis

Synonym(s):

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

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1 G

$28.50

5 G

$136.00

$28.50


Estimated to ship onJanuary 12, 2026Details


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About This Item

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

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Product Name

(S)-(+)-2-Phenylglycinol, 98%

InChI

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

SMILES string

N[C@H](CO)c1ccccc1

InChI key

IJXJGQCXFSSHNL-MRVPVSSYSA-N

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

Quality Level

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This Item
190357429821237647
form

solid

form

-

form

solid

form

powder

assay

98%

assay

98%

assay

99%

assay

99%

optical activity

[α]19/D +33°, c = 0.75 in 1 M HCl

optical activity

[α]24/D −31.7°, c = 0.76 in 1 M HCl

optical activity

[α]19/D +37°, c = 1 in chloroform

optical activity

[α]20/D +155°, c = 1 in 1 M HCl

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

100

mp

75-78 °C (lit.)

mp

75-77 °C (lit.)

mp

136-139 °C (lit.)

mp

>300 °C (lit.)

optical purity

ee: 99% (GLC)

optical purity

ee: 99% (GLC)

optical purity

ee: 99% (GLC)

optical purity

-

Application

Used in a synthesis of chiral, unsymmetrical bisoxazolines.[1]

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Tetrahedron Asymmetry, 17, 2270-2270 (2006)
Jin Han et al.
European journal of medicinal chemistry, 124, 583-607 (2016-09-12)
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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