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14716-89-3

14716-89-3 Structure

14716-89-3 Structure
IdentificationBack Directory
[Name]

(3-METHYLISOXAZOL-5-YL)METHANOL
[CAS]

14716-89-3
[Synonyms]

(3-METHYLISOXAZOL-5-YL)METHANO
5-Isoxazolemethanol, 3-methyl-
(3-Methyl-5-isoxazolyl)methanol
(3-METHYLISOXAZOL-5-YL)METHANOL
3-Methyl-5-isoxazoleMethanol, 97%
(3-methyl-1,2-oxazol-5-yl)methanol
5-(Hydroxymethyl)-3-methylisoxazole
5-(Hydroxymethyl)-3-methylisoxazole97%
5-(Hydroxymethyl)-3-methylisoxazole 97%
(3-methylisoxazol-5-yl)methanol(SALTDATA: FREE)
5-(Hydroxymethyl)-3-methylisoxazole
(3-Methylisoxazol-5-yl)methanol, (3-Methyl-1,2-oxazol-5-yl)methanol
[Molecular Formula]

C5H7NO2
[MDL Number]

MFCD09859210
[MOL File]

14716-89-3.mol
[Molecular Weight]

113.12
Chemical PropertiesBack Directory
[Melting point ]

130 °C
[Boiling point ]

211.82°C (rough estimate)
[density ]

1.1521 g/L at 25℃
[refractive index ]

n/D1.4792
[Fp ]

>110℃
[storage temp. ]

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

liquid
[pka]

13.43±0.10(Predicted)
[color ]

Colourless
[InChI]

1S/C5H7NO2/c1-4-2-5(3-7)8-6-4/h2,7H,3H2,1H3
[InChIKey]

OFSDWHRZVRCPBR-UHFFFAOYSA-N
[SMILES]

CC1=NOC(CO)=C1
Questions And AnswerBack Directory
[Uses]

(Trimethylisoxazole-5-yl)methanol is an alcohol derivative that can be used as a pharmaceutical synthesis intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[WGK Germany ]

3
[HS Code ]

2934999090
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

(3-METHYLISOXAZOL-5-YL)METHANOL(14716-89-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-METHYLISOXAZOLE-5-CARBOXYLIC ACID

4857-42-5

(3-METHYLISOXAZOL-5-YL)METHANOL

14716-89-3

To a solution of tetrahydrofuran (20 mL) containing 3-methylisoxazole-5-carboxylic acid (3 g, 23.6 mmol) was added lithium aluminum hydride (LiAlH4, 1.8 g, 47.37 mmol) in batches at 0 °C and under nitrogen protection. The reaction mixture was stirred at room temperature for 2 hours before water (2 mL) was slowly added to quench the reaction. Subsequently, the mixture was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography with the eluent being a petroleum ether solution of 10%-30% ethyl acetate, resulting in 3-methylisoxazole-5-methanol as a colorless oil (1.5 g, 56% yield). Mass spectrum (ES, m/z) [M+H]+ 114.1; 1H NMR (300 MHz, CDCl3) δ 6.09 (s, 1H), 4.74 (s, 2H), 2.30 (s, 3H), 2.10 (brs, 1H).

[References]

[1] Patent: WO2014/66795, 2014, A1. Location in patent: Paragraph 0175
[2] Patent: WO2016/97870, 2016, A1
[3] ChemMedChem, 2017, vol. 12, # 1, p. 50 - 65
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