(3aR,4R,6S,6aS)-4-(tert-butoxycarbonylaMino)-3-(pentan-3-yl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-6-carboxylic acid - Names and Identifiers
Name | (3aR,4R,6S,6aS)-4-(tert-butoxycarbonylaMino)-3-(pentan-3-yl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-6-carboxylicacid
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Synonyms | (3aR,4R,6S,6aS)-4-(tert-butoxycarbonylaMino)-3-(pentan-3-yl)... (3aR,4R,6S,6aS)-4-(tert-butoxycarbonylaMino)-3-(pentan-3-yl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-6-carboxylicacid (3Ar,4R,6S,6As)-4-(Tert-Butoxycarbonylamino)-3-(Pentan-3-Yl)-4,5,6,6A-Tetrahydro-3Ah-Cyclopenta[D]Isoxazole-6-Carboxylic Acid (3aR,4R,6S,6aS)-4-(tert-butoxycarbonylaMino)-3-(pentan-3-yl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-6-carboxylic acid 2-Methylpropan-2-aMine(3aR,4R,6S)-4-((tert-butoxycarbonyl)aMino)-3-(pentan-3-yl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-6-carboxylate (3aR,4R,6S,6aS)-4-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-(3-pentanyl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d][1,2]oxazole-6-carboxylic acid (3aR,4R,6S,6aS)-4-[(2-methylpropan-2-yl)oxycarbonylamino]-3-pentan-3-yl-4,5,6,6a-tetrahydro-3aH-cyclopenta[d][1,2]oxazole-6-carboxylate,tert-butylazanium
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CAS | 316173-28-1
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EINECS | 1312995-182-4 |
InChI | InChI=1S/C17H28N2O5/c1-6-9(7-2)13-12-11(18-16(22)23-17(3,4)5)8-10(15(20)21)14(12)24-19-13/h9-12,14H,6-8H2,1-5H3,(H,18,22)(H,20,21)/t10-,11+,12+,14+/m0/s1 |
(3aR,4R,6S,6aS)-4-(tert-butoxycarbonylaMino)-3-(pentan-3-yl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-6-carboxylic acid - Physico-chemical Properties
(3aR,4R,6S,6aS)-4-(tert-butoxycarbonylaMino)-3-(pentan-3-yl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d]isoxazole-6-carboxylic acid - Introduction
The compound (3aR,4R,6S,6aS)-4-((tert-butoxycarbonyl) amino)-3-(pentan-3-yl)-4,5,6, 6a-tetrahydro-3ah-cyclopentene [d] isoxazole-6-carboxylic acid (abbreviation: Compound A) is an organic compound. The following is A detailed description of the properties, uses, preparation and safety information of compound A:
Nature:
chemical formula: C13H20N2O4
Molar mass: 272.31g/mol
Appearance: colorless solid
Solubility: Soluble in organic solvents such as dimethyl sulfoxide and dichloromethane; Slightly soluble in water.
Use:
Compound A has A wide range of applications and is often used as A pharmaceutical intermediate and A starting material for organic synthesis. It can be used to synthesize a variety of drugs, pesticides, pigments and functional materials.
Method:
The preparation of compound A is usually carried out by chemical synthesis. Specific preparation methods may vary depending on structural details, but common synthetic steps include:
1. Acid-catalyzed ring-opening reaction of cyclopentanone to produce SEC-butyl alcohol;
2. Reaction of SEC-butyl alcohol with tert-butyl iminoate to generate tert-butoxycarbonyl compound;
3. Schretz alkylation reaction, introduction of pentyl;
4. Isoxazole cyclization reaction to generate isoxazole derivatives of cyclopentanol;
5. Carboxylation reaction, the introduction of carboxyl groups.
Safety Information:
Specific safety information for compound A requires reference to the relevant safety data sheet. In general, the compound should be handled with appropriate personal protective equipment to avoid contact with skin, eyes and mucous membranes. Operate in a well-ventilated area to avoid inhaling dust or vapors. In the use and storage process, to comply with the relevant safety procedures and instructions. If you accidentally come into contact with or breathe this compound, seek medical attention immediately and provide appropriate chemical information.
Last Update:2024-04-09 19:05:49