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Merck
CN

242608

4-乙酰氧基苯甲醛

97%

别名:

对乙酰氧基苯甲醛

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关于此项目

线性分子式:
CH3CO2C6H4CHO
化学文摘社编号:
分子量:
164.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-898-3
MDL number:
Assay:
97%
Form:
liquid
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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

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

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signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

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

法规信息

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历史批次信息供参考:

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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



全球贸易项目编号

货号GTIN
SML0319-10MG04061832075488
SML0319-50MG04061832075495
242608-10G04061836683412