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

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

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-(2-amino-5-oxazolyl)(9CI) is used as a potential pharmaceutical agent for its possible anti-inflammatory, antibacterial, or antifungal properties. Its unique structure and potential biological activities make it a candidate for further research and development in the field of medicine.
Used in Research and Development:
Ethanone, 1-(2-amino-5-oxazolyl)(9CI) is used as a research compound for studying its structure-activity relationship and exploring its potential therapeutic uses. This can help in understanding its full biological potential and pave the way for new drug discoveries and applications in various medical fields.

Upstream product

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

Downstream Products

• 88723-12-0 1-(2-Ethylamino-3H-imidazol-4-yl)-ethanone 
• 92635-35-3 2-Ethylamino-4-methyl-pyrimidin-5-ol 
• 92635-40-0 2-N,N-Dimethylamino-5-hydroxy-4-methylpyrimidine 
• 88723-34-6 1-(2-Dimethylamino-3H-imidazol-4-yl)-ethanone 
• 92635-38-6 2-Amino-5-hydroxy-4-methylpyrimidine 
• 67560-27-4 1-(2-Amino-3H-imidazol-4-yl)-ethanone 
• 92635-44-4 1-H-5-acetyl-2-imidazolone 
• 98455-90-4 2-[N-(3-Phenylpropylamino)]-5-hydroxy-4-methylpyrimidine 
• 98455-89-1 2-[N-(4-phenylbutylamino)]-5-hydroxy-4-methylpyrimidine 
• 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 
• 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 

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.