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(S)-(−)-1-Phenyl-1-propanol

Name: (<I>S</I>)-(−)-1-Phenyl-1-propanol
Brand: ALDRICH

99%

Synonym(s):

(S)-(−)-α-Ethylbenzyl alcohol

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About This Item

Linear Formula:

C₂H₅CH(C₆H₅)OH

CAS Number:

613-87-6

Molecular Weight:

136.19

Beilstein:

2041556

MDL number:

MFCD00066207

UNSPSC Code:

12352002

PubChem Substance ID:

24855518

NACRES:

NA.22

Quality Level

200

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.)

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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Chiral Catalysts & Ligands

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Application

Chiral building block.

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Structure-activity relationships of 1'S-1'-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages.

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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