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147559

Sigma-Aldrich

1-(4-Chlorophenyl)ethanol

98%

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About This Item

Linear Formula:
ClC6H4CH(CH3)OH
CAS Number:
3391-10-4
Molecular Weight:
156.61
EC Number:
222-223-4
MDL number:
MFCD00041038
UNSPSC Code:
12352100
PubChem Substance ID:
24848562
NACRES:
NA.22
form:
liquid
assay:
98%

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.541 (lit.)

bp

119 °C/10 mmHg (lit.)

density

1.171 g/mL at 25 °C (lit.)

functional group

chloro
hydroxyl

SMILES string

CC(O)c1ccc(Cl)cc1

InChI

1S/C8H9ClO/c1-6(10)7-2-4-8(9)5-3-7/h2-6,10H,1H3

InChI key

MVOSNPUNXINWAD-UHFFFAOYSA-N

Application

1-(4-Chlorophenyl)ethanol was used to study transfer dehydrogenation of various alcohols over heterogeneous palladium catalysts using olefins as hydrogen acceptors.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBB0239V
STBB0239
S73693
00329CE
S30562

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Selective transfer dehydrogenation of aromatic alcohols on supported palladium.
Keresszegi C, et al.
New. J. Chem., 25(9), 1163-1167 (2001)
Xiao-Hong Chen et al.
BMC biotechnology, 11, 110-110 (2011-11-22)
Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flavors and functional materials and appropriate whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to these valuable compounds. The recently isolated strain Acetobacter sp. CCTCC M209061 showed exclusive
Xiao-Hong Chen et al.
PloS one, 9(4), e94543-e94543 (2014-04-18)
A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. CCTCC M209061 and enriched 27.5-fold with an overall yield of 0.4% by purification. The enzyme showed a homotetrameric

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