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Merck
CN
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文件

安全信息

242608

Sigma-Aldrich

4-乙酰氧基苯甲醛

97%

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别名:
对乙酰氧基苯甲醛
线性分子式:
CH3CO2C6H4CHO
CAS号:
878-00-2
分子量:
164.16
EC 号:
212-898-3
MDL编号:
MFCD00003384
UNSPSC代码:
12352100
PubChem化学物质编号:
24854572
NACRES:
NA.22

质量水平

100

检测方案

97%

形式

liquid

折射率

n20/D 1.538 (lit.)

bp

152-153 °C/17 mmHg (lit.)

密度

1.168 g/mL at 25 °C (lit.)

SMILES字符串

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

相关类别

一般描述

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

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

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

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

235.4 °F

闪点(°C)

113 °C

个人防护装备

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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