264600-97-7

Basic information

• Product Name: Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI)
• Synonyms: Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI);Isoxazol-3-ylcarbaMic acid tert-butylester;TERT-BUTYL ISOXAZOL-3-YLCARBAMATE
• CAS NO: 264600-97-7
• Molecular Formula: C₈H₁₂N₂O₃
• Molecular Weight: 184.19248
• Product Categories: N-BOC
• Mol File: 264600-97-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI)(264600-97-7)
• EPA Substance Registry System: Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI)(264600-97-7)

Safety Data

• Hazardous Substances Data: 264600-97-7(Hazardous Substances Data)

Usage

General Description

Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) is a chemical compound with the molecular formula C7H11NO3. It is also known by its IUPAC name tert-butyl 3-isoxazolylcarbamate. Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) is commonly used as a reagent in organic synthesis and pharmaceutical research. It is also a precursor in the synthesis of various pharmaceutical drugs. Carbamic acid, 3-isoxazolyl-, 1,1-dimethylethyl ester (9CI) has potential applications in the agricultural industry as well, as it may be used in the development of new pesticides or herbicides. Additionally, it is important to handle this compound with caution, as it may have adverse effects on human health and the environment if not properly managed and disposed of.

Upstream product

• 1750-42-1 3-aminoisoxazole 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 264600-53-5 3-(4-(2-methylimidazol-1-yl)-3-fluorophenyl)-5(R)-(N-(t-butoxycarbonyl)isoxazol-3-yl-aminomethyl)oxazolidin-2-one 
• 264600-52-4 3-(4-(4-hydroxymethylimidazol-1-yl)-3-fluorophenyl)-5(R)-(N-(t-butoxycarbonyl)-isoxazol-3-ylaminomethyl)oxazolidin-2-one 
• 882185-11-7 (5S)-3-{4-[4-(2,1,3-benzoxadiazol-5-yl)piperazin-1-yl]-3-fluorophenyl}-5-[(isoxazol-3-ylamino)methyl]-1,3-oxazolidm-2-one 
• 264600-54-6 3-(4(4-methylimidazol-1-yl)-3-fluorophenyl)-5(R)-(N-(t-butoxycarbonyl)isoxazol-3-yl-aminomethyl)oxazolidin-2-one 
• 501939-83-9 O-tert-butyl (N-(5R)-3-{3-fluoro-4-iodophenyl}-1,3-oxazolidin-2-on-5-yl)methyl N-isoxazol-3-ylcarbamate 
• 264601-10-7 5(R)-((N-isoxazol-3-yl-N-tertbutoxycarbonyl)aminomethyl)-3-(3,5-difluoro-4-(1-(2(R,S)-hydroxy-3-methylthiopropanoyl)-1,2,5,6-tetrahydropyrid-4-yl)phenyl)oxazolidin-2-one 
• 264601-15-2 3-(4-(1-(3-hydroxypropanoyl)-1,2,5,6-tetrahydropyrid-4-yl)-3,5-difluorophenyl)-5(R)-(N-(t-butoxycarbonyl)isoxazol-3-ylaminomethyl)oxazolidin-2-one 
• 1401342-90-2 C₁₈H₁₉BrFN₃O₅ 
• 1443005-68-2 5(R)-(isoxazol-3-yl-N-(tert-butoxycarbonyl)aminomethyl)-3-(3,5-difluoro-4-(2-(tert-butoxycarbonyl)[1,2,5]oxadiazepan-5-yl)phenyl)oxazolidin-2-one 
• 1443005-67-1 5(R)-(isoxazol-3-yl-N-(tert-butoxycarbonyl)aminomethyl)-3-(3,5-difluoro-4-(1-(benzyloxycarbonyl)-2-(tert-butoxycarbonyl)[1,2,5]triazepan-5-yl)phenyl)oxazolidin-2-one 
• 1443005-66-0 5(R)-(isoxazol-3-yl-N-(tert-butoxycarbonyl)aminomethyl)-3-(3-fluoro-4-(1-(benzyloxycarbonyl)-2-(tert-butoxycarbonyl)[1,2,5]triazepan-5-yl)phenyl)oxazolidin-2-one 
• 1364337-88-1 C₂₆H₂₆FN₅O₇ 
• 1219708-23-2 C₃₁H₄₇FN₄O₈Si 
• 1112969-40-0 C₂₄H₂₆F₂N₆O₅ 

Relevant articles and documents

Method for efficiently synthesizing N-3-isooxazole tert-butyl carbamate

The invention discloses a method for efficiently synthesizing N-3-isooxazole tert-butyl carbamate. The synthetic route comprises the following steps: brominating a compound A to obtain a compound B, and reacting the compound B and a compound C to obtain a compound D; and reacting the compound D and di-tert-butyl dicarbonate ester, thereby obtaining the compound E. The reaction formula is as shownin the specification. The process method for synthesizing 3-aminoisoxazole is simple in process, cheap and readily available in raw materials, simple and convenient in operation and extremely suitablefor large-scale industrial production, and has very wide industrial application prospects and market value.

SUBSTITUTED ISOXAZOLES AND THE USE THEREOF AS ANTIBIOTICS

Compounds of formula (I), wherein X is O, S, NH, OCO, NH-CO, NH-COO, NH-CO-NH, NH-CS or NH-CS-NH; R4 is H, (C1-C3)-alkyl optionally substituted by halogen, or a C-linked heterocyclic radical selected from several possibilities; R1 an