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Good factory exports good 3,4-DIETHOXYBENZALDEHYDE 2029-94-9
- Molecular Formula: C11H14 O3
- Molecular Weight: 194.23
- Appearance/Colour: pale yellow liquid
- Vapor Pressure: 0.000862mmHg at 25°C
- Melting Point: 22°C
- Refractive Index: n20/D 1.5570(lit.)
- Boiling Point: 304.7 °C at 760 mmHg
- Flash Point: 129 °C
- PSA: 35.53000
- Density: 1.097
- LogP: 2.29650
3,4-DIETHOXYBENZALDEHYDE(Cas 2029-94-9) Usage
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General Description |
3,4-Diethoxybenzaldehyde is an organic compound with the chemical formula C11H14O3. It is a colorless or light yellow liquid with a floral, sweet, and powdery odor. The compound is used in the pharmaceutical and fragrance industries as a building block for the synthesis of various compounds. It is also used in the creation of perfumes due to its pleasant odor. Additionally, 3,4-Diethoxybenzaldehyde has shown potential as an anti-inflammatory and analgesic agent in various studies, making it a promising candidate for further pharmaceutical development. However, it is important to use this chemical with caution due to its potential to cause skin and eye irritation. |
InChI:InChI=1/C11H14O3/c1-3-13-10-6-5-9(8-12)7-11(10)14-4-2/h5-8H,3-4H2,1-2H3
2029-94-9 Relevant articles
Modular logic gates: Cascading independent logic gates via metal ion signals
Ecik, Esra Tanriverdi,Atilgan, Ahmet,Guliyev, Ruslan,Uyar, T. Bilal,Gumus, Aysegul,Akkaya, Engin U.
, p. 67 - 70 (2014)
Systematic cascading of molecular logic ...
ISOINDOLE DERIVATIVE
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Paragraph 0233; 0237, (2021/02/25)
Disclosed is a compound of formula (I) a...
In vitro study and structure-activity relationship analysis of stilbenoid derivatives as powerful vasorelaxants: Discovery of new lead compound
Chan, Sock Ying,Loh, Yean Chun,Oo, Chuan Wei,Yam, Mun Fei
, (2020/10/12)
The development of vasorelaxant as the a...
Peripheral Substitution of Tetraphenyl Porphyrins: Fine-Tuning Self-Assembly for Enhanced Electroluminescence
Charisiadis, Asterios,Bagaki, Anthi,Fresta, Elisa,Weber, Katharina T.,Charalambidis, Georgios,Stangel, Christina,Hatzidimitriou, Antonios G.,Angaridis, Panagiotis A.,Coutsolelos, Athanassios G.,Costa, Rubén D.
, p. 254 - 265 (2018/04/24)
This study reports the synthesis of two ...
2029-94-9 Process route
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75-03-6
ethyl iodide
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139-85-5
3,4-dihydroxybenzaldehyde
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-
2029-94-9
3,4-diethoxybenzaldehyde
| Conditions | Yield |
|---|---|
|
With
potassium carbonate;
In
acetone;
Reflux;
|
92%
|
|
With
sodium hydroxide; sodium chloride; potassium carbonate;
In
water; N,N-dimethyl-formamide;
|
|
|
With
potassium carbonate;
In
N,N-dimethyl-formamide;
at 20 ℃;
for 17.5h;
|
6.73 g
|
|
With
potassium carbonate;
In
N,N-dimethyl-formamide;
at 20 ℃;
|
-
-
121-32-4
4-hydroxy-3-ethoxybenzaldehyde
-
-
75-03-6
ethyl iodide
-
-
2029-94-9
3,4-diethoxybenzaldehyde
| Conditions | Yield |
|---|---|
|
With
potassium carbonate;
In
dichloromethane; N,N-dimethyl-formamide;
|
2029-94-9 Upstream products
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121-32-4
4-hydroxy-3-ethoxybenzaldehyde
-
64-67-5
diethyl sulfate
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74-96-4
ethyl bromide
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2539-53-9
4-ethoxy-3-hydroxybenzaldehyde
2029-94-9 Downstream products
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92582-04-2
3-((Ξ)-3,4-diethoxy-benzylidene)-dihydro-furan-2-one
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97016-66-5
(3,4-diethoxy-benzyl)-(5-piperidino-pentyl)-amine
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65383-59-7
3,4-diethoxyphenol
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103046-00-0
3,4-diethoxy-4'-phenyl-trans -chalcone