242608
4-Acetoxybenzaldehyde
97%
Synonym(s):
4-Formylphenyl acetate
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10 G
$120.60
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10 G
$120.60
About This Item
Linear Formula:
CH3CO2C6H4CHO
CAS Number:
Molecular Weight:
164.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
97%
form
liquid
refractive index
n20/D 1.538 (lit.)
bp
152-153 °C/17 mmHg (lit.)
density
1.168 g/mL at 25 °C (lit.)
functional group
aldehyde
ester
SMILES string
CC(=O)Oc1ccc(C=O)cc1
InChI
1S/C9H8O3/c1-7(11)12-9-4-2-8(6-10)3-5-9/h2-6H,1H3
InChI key
SEVSMVUOKAMPDO-UHFFFAOYSA-N
Related Categories
General description
The reductive amination of 4-acetoxybenzaldehyde (4-formylphenyl acetate) with an azanonaborane cluster in the presence of H3BNH2(CH2)4NH2 was studied[1].
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Afaf R Genady
Organic & biomolecular chemistry, 3(11), 2102-2108 (2005-05-27)
The reactivity of an azanonaborane cluster containing free amino groups {H2N(CH2)4H2NB8H11NH(CH2)4NH2} towards ketones and aldehydes is investigated. In a one step reaction, the reductive amination of some ketones and aldehydes (namely acetone, benzaldehyde, 3-hydroxybenzaldehyde, 4-hydroxybenzaldehyde, 4-nitrobenzaldehyde, 4-acetoxybenzaldehyde, and 4-acetamidobenzaldehyde) with
Mahmoud H El-Maghrabey et al.
Journal of pharmaceutical and biomedical analysis, 158, 38-46 (2018-06-04)
α-Dicarbonyl compounds (α-DCs) are very clinically important as they are considered as advanced glycation end products (AGEs) precursors and biomarkers for many chronic diseases such as diabetes and vascular diseases, in addition to their major role in progression of complications
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