Name | 3-aminoisoxazole |
Synonyms | 3-aminoisoxazole 3-Amineisoxazole ISOXAZOL-3-AMINE 3-AMINOISOXAZOLE 3-amino isoxazole 1,2-oxazol-3-amine 1,2-benzisoxazol-3-amine 3-Aminoisoxazole3-Isoxazolamine Isoxazol-3-amine, 1,2-Oxazol-3-amine, 3-Amino-1,2-oxazole |
CAS | 1750-42-1 36216-80-5 |
EINECS | 605-748-7 |
InChI | InChI=1/C7H6N2O/c8-7-5-3-1-2-4-6(5)10-9-7/h1-4H,(H2,8,9) |
InChIKey | RHFWLPWDOYJEAL-UHFFFAOYSA-N |
Molecular Formula | C3H4N2O |
Molar Mass | 84.08 |
Density | 1.138g/mLat 25°C(lit.) |
Melting Point | 148-150 °C(Solv: ethyl ether (60-29-7); ligroine (8032-32-4)) |
Boling Point | 226-228°C(lit.) |
Flash Point | >230°F |
Vapor Presure | 0.000559mmHg at 25°C |
Appearance | Liquid |
Color | Clear yellow |
pKa | 2.27±0.10(Predicted) |
Storage Condition | 2-8°C(protect from light) |
Refractive Index | n20/D 1.511(lit.) |
Use | 3-Aminoisoxazole is an organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process. |
Hazard Symbols | Xi - Irritant |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R37/38 - Irritating to respiratory system and skin. R36 - Irritating to the eyes |
Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
HS Code | 29349990 |
Hazard Note | Irritant |
Patent type: invention patent
Application (patent) No.: cn202011109306.2
Application date: 20201016
Publication / Announcement No.: cn112047897a
Date of Publication / announcement: 20201208
Applicant (patentee): Yangzhou Tianhe Pharmaceutical Co., Ltd
Country / Province Code: cn321012
Summary:
The invention belongs to the technical field of medicine, in particular to a preparation method of 3-aminoisoxazole:
(1) Preparation of 2,3 dichloropropionitrile: put acrylonitrile, N, n dimethylformamide and pyridine into the reaction vessel, reduce the temperature to 5 ~ 15 ℃, fill the reaction vessel with chlorine and maintain the reaction temperature of 1020 ℃; After chlorine gas is introduced, the temperature is controlled at 15 ~ 25 ℃ and stirred for 5 hours; Blow out excess chlorine until the reaction solution is yellowish or colorless and transparent to obtain 2,3 dichloropropiononitrile p>
(2) Preparation of 3-aminoisoxazole: under alkaline conditions, 3-aminoisoxazole was synthesized from hydroxyurea and 2,3-dichloropropiononitrile with N, N-dimethylformamide as catalyst The invention is used to solve the technical problem that the preparation of 3-aminoisoxazole adopts 2,3 dibromo propionitrile intermediate, resulting in extremely easy blanking and high process risk p>
Application (patent) No.: cn 200410017060
Date of application: Mar 19, 2004
Publication / Announcement No.: cn 1562985 a
Applicant (patentee): Shanghai Institute of Optics and precision machinery, Chinese Academy of Sciences
Country / Province Code: Shanghai
Summary:
The invention relates to a preparation method of 5-substituted-3-aminoisoxazole compound. The compound has the following general structural formula: in the structural formula, n represents nitrogen, C represents carbon, and R represents 1-4 alkyl groups p>
The preparation method is to first react the substituted acetylacetonitrile with hydroxylamine hydrochloride under weak alkaline conditions to obtain the mixture of aminooxime and the by-product 5-amino-3-substituted isoxazole compound, then remove the by-product by solvent extraction, the aminooxime cyclizes under the action of weak acid, and finally obtain the high-purity 5-substituted-3-amino-isoxazole compound p>
application | 3-aminoisoxazole is an organic synthesis intermediate and a pharmaceutical intermediate, which is mainly used in laboratory research and development and chemical production. |