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256323

Sigma-Aldrich

(S)-(−)-1-Phenyl-1-propanol

99%

Synonym(s):

(S)-(−)-α-Ethylbenzyl alcohol

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About This Item

Linear Formula:
C2H5CH(C6H5)OH
CAS Number:
Molecular Weight:
136.19
Beilstein:
2041556
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

optical activity

[α]20/D −47°, c = 2.25 in hexane

optical purity

ee: 99% (GLC)

refractive index

n20/D 1.520 (lit.)

bp

94-95 °C/10 mmHg (lit.)

density

0.992 g/mL at 25 °C (lit.)

functional group

hydroxyl
phenyl

SMILES string

CC[C@H](O)c1ccccc1

InChI

1S/C9H12O/c1-2-9(10)8-6-4-3-5-7-8/h3-7,9-10H,2H2,1H3/t9-/m0/s1

InChI key

DYUQAZSOFZSPHD-VIFPVBQESA-N

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Application

Chiral building block.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Hisashi Matsuda et al.
Bioorganic & medicinal chemistry letters, 15(7), 1949-1953 (2005-03-23)
1'S-1'-Acetoxychavicol acetate from the rhizomes of Alpinia galanga inhibited nitric oxide (NO) production in lipopolysaccharide-activated mouse peritoneal macrophages with an IC(50) value of 2.3 microM. To clarify the structure-activity relationship of 1'S-1'-acetoxychavicol acetate, various natural and synthetic phenylpropanoids and synthetic

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