87005-17-2

Basic information

• Product Name: Ethanone, 1-(2-amino-5-oxazolyl)- (9CI)
• Synonyms: Ethanone, 1-(2-amino-5-oxazolyl)- (9CI);1-(2-Amino-1,3-oxazol-5-yl)ethanone;1-(2-amino-5-oxazolyl)ethanone;1-(2-aminooxazol-5-yl)ethanone
• CAS NO: 87005-17-2
• Molecular Formula: C₅H₆N₂O₂
• Molecular Weight: 126.11334
• Product Categories: ACETYLGROUP
• Mol File: 87005-17-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethanone, 1-(2-amino-5-oxazolyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(2-amino-5-oxazolyl)- (9CI)(87005-17-2)
• EPA Substance Registry System: Ethanone, 1-(2-amino-5-oxazolyl)- (9CI)(87005-17-2)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 87005-17-2(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-(2-amino-5-oxazolyl)- (9CI) is a chemical compound that belongs to the oxazole class of compounds, which are characterized by a five-membered ring containing oxygen and nitrogen atoms. This particular compound has a unique structure with an amino group attached to a oxazolyl group, giving it potential pharmaceutical applications. It may possess biological activities such as anti-inflammatory, antibacterial, or antifungal properties. Further research on this compound's structure-activity relationship and potential therapeutic uses may reveal its full biological potential.

Upstream product

• 87005-15-0 α-bromoacetoacetaldehyde 
• 57-13-6 urea 
• 82982-63-6 2-bromo-1-hydroxy-3-oxo-1-butene 
• 67-64-1 acetone 

Downstream Products

• 98455-92-6 2-[N-(3-(p-Chlorophenyl)propylamino)]-5-hydroxy-4-methylpyrimidine 
• 98455-88-0 2-[N-(5-Phenylpentylamino)]-5-hydroxy-4-methylpyrimidine 
• 98455-86-8 2-[N-(6-phenylhexylamino)]-5-hydroxy-4-methylpyrimidine 
• 98455-95-9 2-[N-(5-(p-Chlorophenyl)pentylamino)]-5-hydroxy-4-methylpyrimidine 
• 1384275-73-3 2,2'-((5-(1-(((4-(trifluoromethyl)benzyl)oxy)imino)ethyl)oxazol-2-yl)azanediyl)bis(N-((tetrahydro-2H-pyran-4-yl)methyl)acetamide) 
• 1384275-72-2 2,2'-((5-(1-(((4-(trifluoromethyl)benzyl)oxy)imino)ethyl)oxazol-2-yl)azanediyl)diacetic acid 
• 1384276-71-4 diethyl 2,2'-((5-(1-(((4-(trifluoromethyl)benzyl)oxy)imino)ethyl)oxazol-2-yl)azanediyl)diacetate 
• 98456-00-9 2-[4-(3-Phenylpropyl)-N-piperidino]-5-hydroxy-4-methylpyrimidine hydrochloride 
• 98455-89-1 2-[N-(4-phenylbutylamino)]-5-hydroxy-4-methylpyrimidine 
• 98455-98-2 2-(4-Benzyl-N-piperidino)-5-hydroxy-4-methylpyrimidine 
• 98455-90-4 2-[N-(3-Phenylpropylamino)]-5-hydroxy-4-methylpyrimidine 
• 856014-44-3 2-amino-4-(3-bromophenyl)-6-[1-methyl-2-(morpholin-4-yl)-1H-imidazol-4-yl]nicotinonitrile 
• 92635-38-6 2-Amino-5-hydroxy-4-methylpyrimidine 
• 67560-27-4 1-(2-Amino-3H-imidazol-4-yl)-ethanone 

Relevant articles and documents

ANTIULCER 2-GUANIDINO-4-(2-SUBSTITUTED-AMINO-4-IMIDAZOLYL)THIAZOLES AND PROCESS THEREFOR

Heretofore unavailable 2-guanidino-4-(2-substituted-amino-4-imidazolyl) thiazoles; a novel process therefor, also advantageous for the preparation of known antiulcer 2-guanidino-4-(2-substituted-amino-4-imidazolyl) thiazoles; intermediate compounds therefor; and a method for treatment of ulcers in mammals therewith.

SYNTHESIS OF DERIVATIVES OF 3-OXOBUTANAL CONTAINING FUNCTIONAL GROUPS IN THE MESOMETHYLENE UNIT

The synthesis of 2-bromo-3-oxobutanal was realized by the bromination of 1-dialkylamino-1-buten-3-ones.The trans-enol form predominates in solutions.The direct nitration of 1,1-diethoxy-3-butanol leads to 2-nitro-3-oxobutanal.