- CasNo 3788-94-1
- Purity 99%
Location:Home > Agrochemicals
Quality products?make an important contribution to long-term revenue and profitability. Factory supply good quality Ethyl 2-(ethoxymethylene)acetoacetate 3788-94-1 with stock
1.What is the Ethyl 2-(ethoxymethylene)acetoacetate ?
Used in Pharmaceutical Industry:
Ethyl 2-(ethoxymethylene)acetoacetate is used as a reagent for the preparation of various pharmaceuticals. Its unique molecular structure allows for the synthesis of complex organic molecules, which are essential in the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical sector, Ethyl 2-(ethoxymethylene)acetoacetate serves as a precursor in the production of agrochemicals. Its ability to form complex organic molecules makes it a key component in the synthesis of pesticides, herbicides, and other agricultural chemicals.
Used in Flavor and Fragrance Industry:
Ethyl 2-(ethoxymethylene)acetoacetate is used as a precursor in the production of food flavorings and fragrances. Its versatility in organic synthesis enables the creation of a wide range of scents and tastes, enhancing the sensory experience of various food products.
Used in Dye and Pigment Industry:
This chemical compound is also utilized in the manufacture of dyes and pigments. Its role as a starting material for complex organic molecules contributes to the development of vibrant colors and hues used in various applications, including textiles, paints, and plastics.
Regulatory Considerations:
Given the broad applications of Ethyl 2-(ethoxymethylene)acetoacetate, its production and use are closely regulated to ensure safety and environmental protection. This regulation helps mitigate potential risks associated with its strong odor and chemical properties, promoting responsible practices across industries that rely on this versatile compound.
-
-
141-97-9
ethyl acetoacetate
-
-
122-51-0
orthoformic acid triethyl ester
-
-
3788-94-1
2-ethoxymethylene-3-oxobutanoic acid ethyl ester
| Conditions | Yield |
|---|---|
|
With
acetic anhydride;
at 120 ℃;
for 6h;
|
90%
|
|
With
acetic anhydride;
|
87%
|
|
With
acetic anhydride;
at 130 ℃;
for 5h;
|
80%
|
|
With
acetic anhydride;
at 130 ℃;
for 2h;
|
80%
|
|
With
acetic anhydride;
at 130 ℃;
for 12h;
|
79%
|
|
With
acetic anhydride;
Reflux;
|
70%
|
|
With
acetic anhydride;
at 135 ℃;
|
70%
|
|
With
acetic anhydride;
at 120 - 140 ℃;
for 7h;
|
68%
|
|
With
acetic anhydride;
at 130 ℃;
for 4h;
|
65%
|
|
With
acetic anhydride;
KSF Montmorillonite;
at 125 ℃;
for 0.25h;
Further Variations:;
Catalysts;
Product distribution;
microwave irradiation;
|
64%
|
|
at 150 ℃;
|
|
|
In
acetic anhydride;
|
|
|
With
acetic anhydride;
|
|
|
With
acetic anhydride;
for 1h;
Heating;
|
430 g
|
|
With
acetic anhydride;
for 4h;
Heating;
|
|
|
With
acetic anhydride;
at 110 ℃;
for 3h;
|
|
|
In
acetic anhydride;
at 90 - 150 ℃;
for 2.5h;
|
|
|
With
acetic anhydride;
at 20 ℃;
for 4h;
Heating / reflux;
|
|
|
With
acetic anhydride;
at 100 ℃;
for 11h;
|
|
|
With
acetic anhydride;
|
|
|
With
acetic anhydride;
Reflux;
|
|
|
With
propionic acid anhydride;
for 2h;
Reflux;
|
|
|
With
acetic anhydride;
at 120 ℃;
for 10h;
|
|
|
With
acetic anhydride;
for 8h;
|
|
|
With
acetic anhydride;
at 120 ℃;
for 10h;
|
|
|
With
acetic anhydride;
Reflux;
|
|
|
With
acetic anhydride;
|
|
|
With
acetic anhydride;
at 120 ℃;
for 10h;
|
|
|
In
acetic anhydride;
for 8h;
Reflux;
|
|
|
With
acetic anhydride;
for 7h;
Reflux;
|
|
|
With
acetic anhydride;
at 135 ℃;
|
|
|
With
acetic anhydride;
at 130 ℃;
for 12h;
|
-
-
141-97-9
ethyl acetoacetate
-
-
149-73-5
trimethyl orthoformate
-
-
3788-94-1
2-ethoxymethylene-3-oxobutanoic acid ethyl ester
| Conditions | Yield |
|---|---|
|
With
acetic anhydride;
for 2h;
Heating;
|
73%
|
2.What is the CAS number for Ethyl 2-(ethoxymethylene)acetoacetate ?
The CAS number of Ethyl 2-(ethoxymethylene)acetoacetate is 3788-94-1.
More information of Ethyl 2-(ethoxymethylene)acetoacetate 3788-94-1 are:
|
CAS?Number |
3788-94-1 |
|
Density |
1.049 g/cm3 |
|
Boiling Point |
268.8 °C at 760 mmHg |
|
Flash Point |
113.7 °C |
|
Vapor Pressure |
0.00755mmHg at 25°C |
|
Refractive Index |
1.4730 to 1.4770 |
|
HS CODE |
2918990090 |
|
PSA |
52.60000 |
|
LogP |
1.05890 |
3.What are another words for Ethyl 2-(ethoxymethylene)acetoacetate ?
Synonyms?for?Ethyl 2-(ethoxymethylene)acetoacetate 3788-94-1:Acetoaceticacid, 2-(ethoxymethylene)-, ethyl ester (6CI,7CI,8CI);2-(Ethoxymethylene)acetoacetic acid ethyl ester;2-Acetyl-3-ethoxyacrylic acidethyl ester;2-Ethoxymethylene-3-oxobutanoic acid ethyl ester;2-[1-Ethoxymethylidene]-3-oxo-butyric acid ethyl ester;Ethyl(ethoxymethylene)acetoacetate;Ethyl 2-(ethoxymethylene)-3-oxobutyrate;Ethyl2-(ethoxymethylene)acetoacetate;Ethyl 2-acetyl-3-ethoxyacrylate;Ethyl2-ethoxymethylene-3-oxobutanoate;NSC 32775;Ethyl 2-(ethoxymethylene)acetoacetate;
4.What is the molecular formula of Ethyl 2-(ethoxymethylene)acetoacetate?
The chemical formula of ?Ethyl 2-(ethoxymethylene)acetoacetate is?C9H14O4 which containing 9 Carbon atoms,14 Hydrogen atoms and 4 Oxygen atoms,and the molecular weight of??Ethyl 2-(ethoxymethylene)acetoacetate?is 186.208.
5.What is Ethyl 2-(ethoxymethylene)acetoacetate (3788-94-1) used for?
Ethyl 2-(ethoxymethylene)acetoacetate, also known as acetoacetic ethyl ester, is a versatile chemical compound used in organic synthesis. It is a clear, colorless liquid with a strong odor, characterized by its molecular structure containing an acetoacetate group. This feature makes it a valuable starting material for the synthesis of complex organic molecules, contributing to its wide range of applications across different industries.
InChI:InChI=1/C9H14O4/c1-4-12-6-8(7(3)10)9(11)13-5-2/h6H,4-5H2,1-3H3/b8-6-
Relevant articles related to Ethyl 2-(ethoxymethylene)acetoacetate:
|
Article |
Source |
|
Molecular Cobalt Catalysts for O2 Reduction: Low-Overpotential Production of H2O2 and Comparison with Iron-Based Catalysts |
Wang, Yu-Heng,Pegis, Michael L.,Mayer, James M.,Stahl, Shannon S. , p. 16458 - 16461 (2017) |
|
Synthesis and Nematocidal Activity of N-Substituted 3-Methyl-1H-pyrazole-4-carboxamide Derivatives Against Meloidogyne incognita |
Cheng, Long,Shen, Zhong-Hua,Xu, Tian-Ming,Tan, Cheng-Xia,Weng, Jian-Quan,Han, Liang,Peng, Wei-Li,Liu, Xing-Hai , p. 946 - 950 (2018) |
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