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2-Ethoxybenzaldehyde

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CAS:613-69-4
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  • 2-Ethoxybenzaldehyde
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  • CAS:613-69-4
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  • CAS:613-69-4
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  • Purity: 99%
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  • 2-Ethoxybenzaldehyde
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  • 2025-01-03
  • CAS:613-69-4
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2-Ethoxybenzaldehyde Basic information
Product Name:2-Ethoxybenzaldehyde
Synonyms:2-ETHOXYBENZALDEHYDE;Benzaldehyde, o-ethoxy-;AKOS BBS-00003145;AKOS B029848;ASISCHEM R42365;LABOTEST-BB LT00616095;SALICYLALDEHYDE ETHYL ETHER;O-ETHOXYBENZALDEHYDE
CAS:613-69-4
MF:C9H10O2
MW:150.17
EINECS:210-349-2
Product Categories:Aromatic Aldehydes & Derivatives (substituted);Aldehydes;C9;Carbonyl Compounds
Mol File:613-69-4.mol
2-Ethoxybenzaldehyde Structure
2-Ethoxybenzaldehyde Chemical Properties
Melting point 20-22 C
Boiling point 136-138 °C/24 mmHg (lit.)
density 1.074 g/mL at 25 °C (lit.)
refractive index n20/D 1.543(lit.)
Fp 197 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceLight yellow to yellow Liquid
Sensitive Air Sensitive
BRN 1937270
LogP2.250 (est)
CAS DataBase Reference613-69-4(CAS DataBase Reference)
NIST Chemistry ReferenceBenzaldehyde, 2-ethoxy-(613-69-4)
EPA Substance Registry SystemBenzaldehyde, 2-ethoxy- (613-69-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39-37/39-36
WGK Germany 3
TSCA Yes
HS Code 29122990
MSDS Information
ProviderLanguage
2-Ethoxybenzaldehyde English
ACROS English
SigmaAldrich English
ALFA English
2-Ethoxybenzaldehyde Usage And Synthesis
Chemical Propertiesclear yellow to light brown liquid
Uses2-Ethoxybenzaldehyde was used to study the 1,3-dipolar cycloaddition reactions.
Synthesis Reference(s)Synthetic Communications, 19, p. 3407, 1989 DOI: 10.1080/00397918908052747
Synthesis
2-ETHOXYBENZYL ALCOHOL

71672-75-8

2-Ethoxybenzaldehyde

613-69-4

The general procedure for the synthesis of 2-ethoxybenzaldehyde from o-ethoxybenzyl alcohol was as follows: first, o-ethoxybenzyl alcohol (100 mg, 0.818 mmol), SS-Pd catalyst (918 mg, containing 0.04 mmol Pd), and 3 ml of toluene were mixed and the reaction mixture was purged with molecular oxygen. Subsequently, the reaction was stirred at 110 °C for 5 h, during which the reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was cooled to room temperature, diluted with ethyl acetate and filtered through a cotton bed. The combined organic layers were concentrated by evaporation under reduced pressure and the crude product obtained was purified by silica gel (60-120 mesh) column chromatography (eluent was 95:5 hexane/ethanol solvent mixture) to give 2-ethoxybenzaldehyde (94 mg, 96% yield) as a colorless liquid.

References[1] Tetrahedron Letters, 2001, vol. 42, # 31, p. 5199 - 5201
[2] Tetrahedron Letters, 2013, vol. 54, # 23, p. 2924 - 2928
[3] Tetrahedron Letters, 2011, vol. 52, # 38, p. 4954 - 4956
[4] Canadian Journal of Chemistry, 2008, vol. 86, # 8, p. 782 - 790
2-Ethoxybenzaldehyde Preparation Products And Raw materials
Raw materialsBromoethane-->Salicylaldehyde-->2-ETHOXYBENZYL ALCOHOL-->Iodoethane-->Toluene-->Oxygen
Preparation Products2-ETHOXYCINNAMIC ACID-->2-Ethoxybenzamide-->3-(3-ETHOXYPHENYL)PROPIONIC ACID
Tag:2-Ethoxybenzaldehyde(613-69-4) Related Product Information
4-Dimethylaminobenzaldehyde 2-Nitrobenzaldehyde 4-Hydroxybenzaldehyde Salicylaldehyde 2-(Trifluoromethyl)benzaldehyde 3-Methoxybenzaldehyde o-Anisaldehyde Benzaldehyde 2-Ethoxyphenol Ethoxyquin p-Anisaldehyde 2-Ethoxybenzoic acid KHELLIN MERSALYL ACID NAPHTHOL AS ACETATE sodium benzaldehyde-o-sulfonate O-ACETYLSALICYLOYL CHLORIDE Rotenone

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