Details
Buy Quality 2-Formylbenzoic acid ethyl ester 34046-43-0 In Stock with Immediately Delivery
- Molecular Formula:C10H10O3
- Molecular Weight:178.188
- Vapor Pressure:0.002mmHg at 25°C
- Refractive Index:1.548
- Boiling Point:294.176 °C at 760 mmHg
- Flash Point:128.545 °C
- PSA：43.37000
- Density:1.146 g/cm3
- LogP:1.67580
2-Formylbenzoic acid ethyl ester(Cas 34046-43-0) Usage
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General Description |
2-Formylbenzoic acid ethyl ester, also known as ethyl 2-formylbenzoate, is a chemical compound with the molecular formula C10H10O3. It is a derivative of benzoic acid and has a white crystalline appearance. 2-Formylbenzoic acid ethyl ester is often used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It is also commonly used as a flavoring agent in the food industry. Its chemical properties make it an important reagent in organic chemistry, particularly in the production of esters, aldehydes, and carboxylic acids. Its versatility and relatively stable nature make it a valuable component in the manufacturing of various products. |
InChI:InChI=1/C10H10O3/c1-2-13-10(12)9-6-4-3-5-8(9)7-11/h3-7H,2H2,1H3
34046-43-0 Relevant articles
THIAZOLE DERIVATIVE AND APPLICATIONS
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Paragraph 0099-0100, (2019/04/16)
A thiazole derivative serving as a DHODH...
Nickel-catalyzed reductive defunctionalization of esters in the absence of an external reductant: Activation of C-O bonds
Iyori, Yasuaki,Takahashi, Kenjiro,Yamazaki, Ken,Ano, Yusuke,Chatani, Naoto
supporting information, p. 13610 - 13613 (2019/11/14)
The nickel-catalyzed reductive cleavage ...
Cobalt(ii)-catalyzed benzylic oxidations with potassium persulfate in TFA/TFAA
Li, Tianlei,Li, Jishun,Zhu, Zihao,Pan, Weidong,Wu, Song
, p. 20879 - 20883 (2019/07/12)
A cobalt-catalyzed C(sp3)-H oxygenation ...
6,5-BICYCLIC OCTAHYDROPYRROLOPYRIDINE OREXIN RECEPTOR ANTAGONISTS
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Page/Page column 45, (2016/07/05)
The present invention is directed to 6,5...
34046-43-0 Process route
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75-03-6
ethyl iodide
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119-67-5
o-carboxybenzaldehyde
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34046-43-0
ethyl 2-formylbenzoate
| Conditions | Yield |
|---|---|
|
With
potassium carbonate;
In
N,N-dimethyl-formamide;
at 20 ℃;
|
98% |
|
With
caesium carbonate;
In
N,N-dimethyl-formamide;
at 70 ℃;
for 4h;
|
79% |
|
With
potassium carbonate;
In
N,N-dimethyl-formamide;
at 20 ℃;
|
68% |
|
With
potassium carbonate;
In
butanone;
|
|
|
With
sodium hydrogencarbonate;
In
N-methyl-acetamide;
|
|
|
With
potassium carbonate;
In
N,N-dimethyl-formamide;
for 4h;
Reflux;
|
|
|
With
potassium carbonate;
In
N,N-dimethyl-formamide;
for 4h;
Reflux;
|
|
|
With
potassium carbonate;
In
acetone;
at 70 ℃;
|
|
|
With
potassium carbonate;
In
acetone;
at 70 ℃;
|
|
|
With
potassium carbonate;
In
acetone;
at 70 ℃;
|
|
|
With
potassium carbonate;
In
acetone;
at 70 ℃;
|
-
-
64-67-5
diethyl sulfate
-
-
119-67-5
o-carboxybenzaldehyde
-
-
34046-43-0
ethyl 2-formylbenzoate
| Conditions | Yield |
|---|---|
|
With
potassium hydroxide;
Aliquat 336;
Yield given. Multistep reaction;
1.) 60 deg C, 0.1 Torr, 6 h, 2.) room temp., 18 h;
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With
potassium hydroxide; Aliquat 336;
|
|
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With
triethylamine;
In
dichloromethane;
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34046-43-0 Upstream products
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119-67-5
o-carboxybenzaldehyde
-
75-03-6
ethyl iodide
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27332-37-2
ethyl cyclohepta-2,4,6-trienecarboxylate
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88674-90-2
ethyl 2-(2-hydroxybenzylidine)-hydrazine carboxylate
34046-43-0 Downstream products
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83465-27-4
(3-oxo-1,3-dihydro-isobenzofuran-1-yl)acetic acid ethyl ester
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142671-81-6
ethyl 2-(1,3-dithian-2-yl)benzoate
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136391-65-6
-
223742-36-7
2-[(E)-2-(2,6,6-Trimethyl-cyclohex-1-enyl)-vinyl]-benzoic acid ethyl ester
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