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ASISCHEM N42746

3-ethoxy-4-methoxybenzaldehyde

CAS: 1131-52-8

Molecular Formula: C10H12O3

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ASISCHEM N42746 - Names and Identifiers

Name 3-ethoxy-4-methoxybenzaldehyde
Synonyms AKOS 235-18
AKOS B004408
ASISCHEM N42746
AKOS BBS-00006639
3-ETHOXY-P-ANISALDEHYDE
3-ethyl-4-methoxybenzaldehyde
3-ethoxy-4-methoxybenzaldehyde
3-ETHOXY-4-METHOXYBENZALDEHYDE
CAS 1131-52-8
EINECS 642-869-4
InChI InChI=1/C10H12O2/c1-3-9-6-8(7-11)4-5-10(9)12-2/h4-7H,3H2,1-2H3
InChIKey VAMZHXWLGRQSJS-UHFFFAOYSA-N

ASISCHEM N42746 - Physico-chemical Properties

Molecular FormulaC10H12O3
Molar Mass180.2
Density1.088±0.06 g/cm3(Predicted)
Melting Point51 °C
Boling Point155°C/10mmHg(lit.)
Flash Point113°C
Solubility Soluble in methanol.
Vapor Presure0.01mmHg at 25°C
AppearanceSolid
ColorWhite to Orange to Green
Storage Conditionroom temp
SensitiveAir Sensitive
Refractive Index1.536
MDLMFCD00010128

ASISCHEM N42746 - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Safety DescriptionS23 - Do not breathe vapour.
S24/25 - Avoid contact with skin and eyes.
WGK Germany3
HS Code29124990
Hazard ClassIRRITANT

ASISCHEM N42746 - Reference Information

introduction 3-ethoxy-4-methoxybenzaldehyde is slightly soluble in water and miscible in ethanol, ether, benzene and chloroform. it is a daily chemical essence and an organic intermediate in pharmaceutical chemistry.
Use 3-ethoxy-4-methoxybenzaldehyde is an intermediate in the synthesis of flavors and drug molecules. In addition, in the synthesis and transformation, it mainly revolves around the benzene ring. The aldehyde group is a universal functional group conversion group, which can be easily converted into hydroxyl, cyano, carboxyl, and enamine and imine structures.
synthesis method
3-ethoxy -4-hydroxybenzaldehyde
(2 mmol), tetramethylammonium chloride (2.5 mmol), anhydrous cesium carbonate (2.5 mmol) and 1, 2-dimethoxyethane (2 mL) are added to the
10-mL microwave reaction container, and the reaction container is purged with argon before closing, the mixture in the microwave reactor was irradiated with magnetic stirring at 145°C for 60 minutes (microwave power limit set to 100
W), the container was discharged in a fume hood to remove trimethylamine, the reaction mixture was diluted with ethyl acetate (5 mL), the solids were filtered, the solids were washed with additional ethyl acetate (25
mL), and the filtrate was evaporated in vacuum. Using petroleum ether/ether as eluent, the residue was separated by column chromatography to obtain the target product 3-ethoxy-4-methoxybenzaldehyde.

Figure 13-Ethoxy-4-methoxybenzaldehyde synthesis route
Last Update:2024-04-09 21:01:54
ASISCHEM N42746
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CAS: 1131-52-8
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
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CAS: 1131-52-8
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Product Name: 3-Ethoxy-4-methoxybenzaldehyde Visit Supplier Webpage Request for quotation
CAS: 1131-52-8
Tel: +86 0571-86722205
Email: sales@chinaskyrun.com
Mobile: +8618958170122
QQ: 2531159185 Click to send a QQ messageSend QQ message
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Shanghai Yuanye Bio-Technology Co., Ltd.
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ASISCHEM N42746
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