3-Methyl-1,2-benzisoxazol-6-ol

3-Methyl-1,2-benzisoxazol-6-ol Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
Tel: 13761987713
Email: hxzheng@sunwaypharm.cn
Company Name: Shanghai Jian Chao Chemical Technology Co., Ltd.  
Tel: 150-2103-5486 18017383231
Email: 983544897@qq.com
Company Name: Shanghai Keepontech Co.,Ltd  
Tel: 021-54849683 13601642561
Email: sales@keepontech.com
Company Name: Chengdu AstaTech Trading Co., Ltd./AstaTech (Chengdu) Pharma. Co., Ltd.  
Tel: +86-28-85122536 85324413
Email: market@astatech.cn
3-Methyl-1,2-benzisoxazol-6-ol Basic information
Product Name:3-Methyl-1,2-benzisoxazol-6-ol
Synonyms:6-Hydroxy-3-methylbenzoisoxazole;3-methyl-1,2-benzisoxazol-6-ol(SALTDATA: FREE);1,2-Benzisoxazol-6-ol, 3-methyl-;3-Methyl-1,2-benzisoxazol-6-ol
CAS:66033-92-9
MF:C8H7NO2
MW:149.15
EINECS:
Product Categories:
Mol File:66033-92-9.mol
3-Methyl-1,2-benzisoxazol-6-ol Structure
3-Methyl-1,2-benzisoxazol-6-ol Chemical Properties
storage temp. Inert atmosphere,Room Temperature
AppearanceLight brown to brown Solid
Safety Information
HazardClass IRRITANT
MSDS Information
3-Methyl-1,2-benzisoxazol-6-ol Usage And Synthesis
Synthesis
2,4-DIHYDROXYACETOPHENONE OXIME

6134-79-8

3-METHYL-1,2-BENZISOXAZOL-6-OL

66033-92-9

The general procedure for the synthesis of 3-methyl-6-hydroxybenzisoxazole from the compound (CAS: 6134-79-8) was as follows: 2.0 mmol of 2-hydroxy aryl aldoxime or ketoxime was dissolved in 5 mL of anhydrous dichloromethane (DCM) in an oven-dried round-bottom flask. Under nitrogen protection, 2.0 mmol of DCM solution of trifluoromethanesulfonic anhydride was slowly added to the reaction mixture, and the titration process lasted for 15 minutes. The reaction mixture was stirred at room temperature and the reaction process was monitored by thin layer chromatography (TLC) and gas chromatography-mass spectrometry (GC-MS) (see Table 1). Upon completion of the reaction, the reaction mixture was poured into 100 mL of crushed ice and neutralized with 20 mL of 10% sodium bicarbonate (NaHCO3) solution, followed by extraction with 315 mL of DCM. The pure product was isolated by column chromatography using hexane-ethyl acetate (80:20, v/v) as eluent. All the synthesized 1,2-benzisoxazole derivatives were characterized by GC-MS, nuclear magnetic resonance hydrogen spectroscopy (1H NMR) and carbon spectroscopy (13C NMR) as well as elemental analysis and the obtained data were validated by comparing them with real samples.

References[1] Tetrahedron Letters, 2006, vol. 47, # 47, p. 8247 - 8250
[2] Synthetic Communications, 2014, vol. 44, # 4, p. 547 - 555
[3] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1980, vol. 19, # 7, p. 571 - 575
[4] Patent: CN104945415, 2017, B
Tag:3-Methyl-1,2-benzisoxazol-6-ol(66033-92-9) Related Product Information
(6-Methoxybenzo[d]isoxazol-3-yl)methanamine 3-(4-Methoxy-phenyl)-benzo[d]isoxazol-6-ol 2-(6-Methoxybenzo[d]isoxazol-3-yl)acetic acid 6-Methoxybenzo[d]isoxazole-3-carbonitrile 3-(4-Chloro-phenyl)-benzo[d]isoxazol-6-ol Ethyl 6-hydroxybenzo[d]isoxazole-3-carboxylate 2-(6-Methoxybenzo[d]isoxazol-3-yl)ethanol Methyl 2-(6-methoxybenzo[d]isoxazol-3-yl)acetate 6-Methoxybenzo[d]isoxazole-3-carboxylic acid 1,2-Benzisoxazole, 6-methoxy-3-methyl- 3-Methyl-1,2-benzisoxazol-6-ol 1,2-Benzisoxazol-6-ol ethyl 6-methoxybenzo[d]isoxazole-3-carboxylate AA 193 Brocrinat