ChemicalBook--->CAS DataBase List--->54593-26-9

54593-26-9

54593-26-9 Structure

54593-26-9 Structure
IdentificationMore
[Name]

3,5-DIMETHYL-4-ISOXAZOLECARBALDEHYDE
[CAS]

54593-26-9
[Synonyms]

3,5-DIMETHYL-4-FORMYLISOXAZOLE
3,5-DIMETHYL-4-ISOXAZOLECARBALDEHYDE
3,5-DIMETHYL-4-ISOXAZOLECARBOXALDEHYDE
3,5-DIMETHYL-ISOXAZOLE-4-CARBALDEHYDE
AKOS PAO-1553
BUTTPARK 97\06-58
3,5-Dimethylisoxazole-4-carboxaldehyde
[Molecular Formula]

C6H7NO2
[MDL Number]

MFCD02681977
[Molecular Weight]

125.13
[MOL File]

54593-26-9.mol
Chemical PropertiesBack Directory
[Melting point ]

54-56°C
[Boiling point ]

54-56
[density ]

1.140±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

Solid
[pka]

-2.50±0.28(Predicted)
[color ]

White to Almost white
[CAS DataBase Reference]

54593-26-9(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29349990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrochloric acid-->Ethyl acetate-->Formaldehyde-->Potassium dichromate-->3,5-Dimethylisoxazole-->ADOGEN(R) 464-->(3,5-Dimethyl-4-isoxazolyl)methanol-->Dess-Martin periodinane-->Dichloromethane
Hazard InformationBack Directory
[Chemical Properties]

Off-white solid
[Synthesis]

(3,5-DIMETHYL-4-ISOXAZOLYL)METHANOL

19788-36-4

3,5-DIMETHYL-4-ISOXAZOLECARBALDEHYDE

54593-26-9

General procedure for the synthesis of 3,5-dimethyl-4-isoxazole formaldehyde from 3,5-dimethyl-4-hydroxymethylisoxazole: To a solution of (3,5-dimethylisoxazol-4-yl)methanol (1.00 g, 7.86 mmol) in dichloromethane (20 mL) was slowly added Dess-Martin periodinane (4.17 g, 9.83 mmol) over 10 min at 0 °C. 9.83 mmol) over 10 minutes. The reaction mixture was gradually warmed to room temperature and stirred continuously at this temperature for 60 minutes. After completion of the reaction, the mixture was filtered through diatomaceous earth (Celite) and washed with dichloromethane. The collected organic layer was dried over anhydrous sodium sulfate and subsequently concentrated under reduced pressure. The crude product was purified by column chromatography (eluent: 15% ethyl acetate/hexane) to afford the target product 3,5-dimethyl-4-isoxazolecarboxaldehyde (0.450 g, 46% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 9.92 (s, 1H), 2.68 (s, 3H), 2.31 (s, 3H).

[References]

[1] Organic Preparations and Procedures International, 2003, vol. 35, # 2, p. 207 - 214
[2] Synthetic Communications, 1983, vol. 13, # 10, p. 817 - 822
[3] Patent: WO2013/19635, 2013, A1. Location in patent: Page/Page column 71
[4] Patent: WO2013/19682, 2013, A1. Location in patent: Page/Page column 92
[5] Patent: WO2013/19626, 2013, A1. Location in patent: Page/Page column 26
Spectrum DetailBack Directory
[Spectrum Detail]

3,5-DIMETHYL-4-ISOXAZOLECARBALDEHYDE(54593-26-9)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

3,5-dimethyl-4-isoxazolecarbaldehyde(54593-26-9)
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