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282693

Sigma-Aldrich

(S)-(+)-2-Phenylglycinol

98%, for peptide synthesis

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:
3196190
MDL number:
MFCD00064404
UNSPSC Code:
12352209
PubChem Substance ID:
24857063
NACRES:
NA.22

product name

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

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 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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Sigma-Aldrich

P25485

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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
Tetrahedron Asymmetry, 17, 2270-2270 (2006)

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