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242608

4-Acetoxybenzaldehyde

Name: 4-Acetoxybenzaldehyde
Brand: ALDRICH

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

NACRES:

NA.22

PubChem Substance ID:

24854572

UNSPSC Code:

12352100

EC Number:

212-898-3

MDL number:

MFCD00003384

Assay:

97%

Form:

liquid

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Properties

Quality Level

100

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

Description

General description

The reductive amination of 4-acetoxybenzaldehyde (4-formylphenyl acetate) with an azanonaborane cluster in the presence of H₃BNH₂(CH₂)₄NH₂ was studied.

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

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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Synthesis and characterization of a novel functionalized azanonaborane cluster for boron neutron capture therapy.

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

Aromatic aldehydes as selective fluorogenic derivatizing agents for α-dicarbonyl compounds. Application to HPLC analysis of some advanced glycation end products and oxidative stress biomarkers in human serum.

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

Global Trade Item Number

SKU	GTIN
SML0319-50MG	04061832075495
SML0319-10MG	04061832075488
242608-10G	04061836683412