43214-88-6

Basic information

• Product Name: 5-Isoxazolemethanol,3-methyl-,acetate(ester)(9CI)
• Synonyms: 5-Isoxazolemethanol,3-methyl-,acetate(ester)(9CI);5-IsoxazoleMethanol,3-Methyl-, 5-acetate;3-Methyl-5-isoxazolemethanol acetate;(3-METHYL-1,2-OXAZOL-5-YL)METHYL ACETATE
• CAS NO: 43214-88-6
• Molecular Formula: C₇H₉NO₃
• Molecular Weight: 155.15
• EINECS: 200-258-5
• Product Categories: OXAZOLE
• Mol File: 43214-88-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 65-73℃ (2 Torr)
• Flash Point: 92.9±23.2℃
• Appearance: /
• Density: 1.153±0.06 g/cm3 (20 ºC 760 Torr)
• Storage Temp.: Amber Vial, -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform, Methanol
• PKA: -1.87±0.10(Predicted)
• Stability: Moisture and Acid Sensitive
• CAS DataBase Reference: 5-Isoxazolemethanol,3-methyl-,acetate(ester)(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Isoxazolemethanol,3-methyl-,acetate(ester)(9CI)(43214-88-6)
• EPA Substance Registry System: 5-Isoxazolemethanol,3-methyl-,acetate(ester)(9CI)(43214-88-6)

Safety Data

• Hazardous Substances Data: 43214-88-6(Hazardous Substances Data)

Usage

Uses

3-Methyl-5-isoxazolemethanol acetate is a compound with an oxazole group that is known to contribute to agonist characteristics relating to glutamic acid.

Upstream product

• 40340-41-8 5-chloromethyl-3-methylisoxazole 
• 127-09-3 sodium acetate 

Downstream Products

• 1505453-59-7 2-((4S)-6-(4-chlorophenyl)-1-methyl-8-(1-methyl-1H-pyrazol-4-yl)-4H-benzo[c]isoxazolo[4,5-e]azepin-4-yl)acetamide 
• 1505453-81-5 C₂₆H₂₄ClN₅O₂ 
• 1380089-79-1 methyl 2-(5-((E)-(((S)-tert-butylsulfinyl)imino)methyl)-3-methylisoxazol-4-yl)-5-chlorobenzoate 
• 1380089-77-9 2-((6S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-isoxazolo[5,4-c]thieno[2,3-e]azepin-6-yl)-N-(2,2-dimethoxyethyl)acetamide 
• 1380089-76-8 2-((6S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-isoxazolo[5,4-c]thieno[2,3-e]azepin-6-yl)ethanethioamide 
• 1380088-19-6 2-((6S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-isoxazolo[5,4-c]thieno[2,3-e]azepin-6-yl)-N-ethylacetamide 
• 1380087-45-5 2-((6S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-isoxazolo[5,4-c]thieno[2,3-e]azepin-6-yl)acetamide 
• 1448631-44-4 C₂₄H₂₅ClN₂O₃S 

Relevant articles and documents

Reaction of 3-alkyl(aryl)-5-chloromethylisoxazoles with nucleophilic reagents

Previously unknown 3-alkyl(aryl)isoxazoles containing various functional groups in the 5-position were synthesized by reactions of 3-alkyl(aryl)-5- chloromethylisoxazoles with nucleophiles (2-aminoethanol, methylamine, sodium acetate, and sodium methoxide). Pleiades Publishing, Ltd., 2011.