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432881

Sigma-Aldrich

4-(Chloromethyl)phenyl acetate

98%

Sinónimos:

α-Chloro-p-cresol acetate, 4-Acetoxybenzyl chloride, p-(Chloromethyl)phenyl acetate, p-Acetoxybenzyl chloride

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About This Item

Fórmula lineal:
CH3CO2C6H4CH2Cl
Número de CAS:
39720-27-9
Peso molecular:
184.62
MDL number:
MFCD00209564
UNSPSC Code:
12352100
PubChem Substance ID:
24867105
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.53 (lit.)

bp

240 °C (lit.)

density

1.201 g/mL at 25 °C (lit.)

SMILES string

CC(=O)Oc1ccc(CCl)cc1

InChI

1S/C9H9ClO2/c1-7(11)12-9-4-2-8(6-10)3-5-9/h2-5H,6H2,1H3

InChI key

OKRCXSCDWKJWSW-UHFFFAOYSA-N

Application

4-(Chloromethyl)phenyl acetate may be used as reagent in 4-(chloromethyl)phenyl acetate assay.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Accumulating evidence suggests that TNF-α-mediated immune-neurotoxicity contributes to cognitive impairments and the overall severity of schizophrenia (OSOS). There are no data whether peripheral IL-6 and IL-4 may affect the phenome of schizophrenia above and beyond the effects of TNF-α and
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Accumulating evidence shows that nitro-oxidative pathways play an important role in the pathophysiology of major depressive disorder (MDD) and bipolar disorder (BD) and maybe anxiety disorders. The current study aims to examine superoxide dismutase (SOD1), catalase, lipid hydroperoxides (LOOH), nitric
Estefania Gastaldello Moreira et al.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry, 20(5), 368-380 (2017-04-27)
Objectives: Mood disorders (MDs) frequently co-exist with cardiovascular disease (CVD) and immune-inflammatory and oxidative stress are important shared pathophysiological pathways. Even though there has been an extensive investigation of the enzyme paraoxonase 1 (PON1) as a biomarker of susceptibility for
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