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242608

Sigma-Aldrich

4-Acetoxybenzaldehyde

97%

Synonym(s):

4-Formylphenyl acetate

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About This Item

Linear Formula:
CH3CO2C6H4CHO
CAS Number:
878-00-2
Molecular Weight:
164.16
EC Number:
212-898-3
MDL number:
MFCD00003384
UNSPSC Code:
12352100
PubChem Substance ID:
24854572
NACRES:
NA.22

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

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCL3571
MKCF8966
MKCB9250
MKBT3624V
MKBL2987V

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Sigma-Aldrich

A1800

4-Acetamidobenzaldehyde

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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