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Factory supply 2-Ethoxybenzoyl chloride 42926-52-3 with low price
- Molecular Formula: C9H9ClO2
- Molecular Weight: 184.622
- Appearance/Colour: COLORLESS TO YELLOW TO BROWN LIQUID
- Vapor Pressure: 0.00677mmHg at 25°C
- Refractive Index: 1.553
- Boiling Point: 270.6 °C at 760 mmHg
- Flash Point: 100.8 °C
- PSA： 26.30000
- Density: 1.18 g/cm3
- LogP: 2.46430
2-Ethoxybenzoyl chloride(Cas 42926-52-3) Usage
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General Description |
2-Ethoxybenzoyl chloride is a chemical compound with the molecular formula C10H11ClO2. It is a colorless to pale yellow liquid that is used as a reagent in organic synthesis for the preparation of esters, amides, and carboxylic acids. It is a versatile and reactive compound that is commonly used in the pharmaceutical and agrochemical industries. 2-Ethoxybenzoyl chloride is a key intermediate in the synthesis of various pharmaceutical compounds and is also used as a coupling agent in the production of dyes and pigments. It is important to handle this compound with caution, as it is corrosive and can cause severe skin and eye irritation upon contact. |
InChI:InChI=1/C9H9ClO2/c1-2-12-8-6-4-3-5-7(8)9(10)11/h3-6H,2H2,1H3
42926-52-3 Relevant articles
Process for preparing O-ethoxybenzoic acid chloride (by machine translation)
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, (2020/08/26)
The method comprises the following steps...
Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide
Jevti?, Ivana I.,Do?en-Mi?ovi?, Ljiljana,Ivanovi?, Evica R.,Ivanovi?, Milovan D.
, p. 1550 - 1560 (2016/06/01)
An efficient, one-pot procedure for the ...
Sedinafine derivatives of the microwave-assisted method for preparing
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Paragraph 0061, (2016/12/07)
The invention discloses a microwave-assi...
METHOD FOR PRODUCING OXAZOLE COMPOUND
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Page/Page column 73-74, (2014/03/25)
An object of the present invention is to...
42926-52-3 Process route
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119-36-8,8024-54-2
methyl salicylate
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42926-52-3
2-ethoxybenzoyl chloride
| Conditions | Yield |
|---|---|
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Multi-step reaction
with
3
steps
1.1: potassium hydroxide / acetone / 0.5 h / 20 °C
1.2: Reflux
2.1: methanol; sodium hydroxide / 50 °C
3.1: N,N-dimethyl-formamide; phosgene / acetone / 50 °C
With
methanol; phosgene; N,N-dimethyl-formamide; potassium hydroxide; sodium hydroxide;
In
acetone;
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42926-52-3
2-ethoxybenzoyl chloride
| Conditions | Yield |
|---|---|
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42926-52-3 Upstream products
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134-11-2
2-ethoxybenzoic acid
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119-36-8
methyl salicylate
42926-52-3 Downstream products
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16386-47-3
2-ethoxy-benzoic acid benzo[1,3]dioxol-5-yl ester
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112819-13-3
2-ethoxy-benzoic acid-(1-phenyl-2-pyrrolidino-ethyl ester); hydrochloride
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102476-73-3
2-ethoxy-benzoic acid-(1-phenyl-2-piperidino-ethyl ester); hydrochloride
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105541-36-4
2,5-bis-[4-(2-ethoxy-benzoylamino)-phenyl]-furan
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