3916-80-1

Basic information

• Product Name: N-(5-Phenyl-1,3,4-oxadiazol-2-yl)acetamide
• Synonyms: N-(5-Phenyl-1,3,4-oxadiazol-2-yl)acetamide
• CAS NO: 3916-80-1
• Molecular Formula: C₁₀H₉N₃O₂
• Molecular Weight: 203.1974
• Mol File: 3916-80-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.293g/cm³
• Refractive Index: 1.598
• CAS DataBase Reference: N-(5-Phenyl-1,3,4-oxadiazol-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(5-Phenyl-1,3,4-oxadiazol-2-yl)acetamide(3916-80-1)
• EPA Substance Registry System: N-(5-Phenyl-1,3,4-oxadiazol-2-yl)acetamide(3916-80-1)

Safety Data

• Hazardous Substances Data: 3916-80-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H9N3O2/c1-7(14)11-10-13-12-9(15-10)8-5-3-2-4-6-8/h2-6H,1H3,(H,11,13,14)

Upstream product

• 141-78-6 ethyl acetate 
• 58975-55-6 N-(2-benzoylhydrazine-1-carbonothioyl)benzamide 
• 5351-66-6 benzoyl thiosemicarbazide 
• 58455-03-1 3-(benzoylamino)-5-methyl-1,2,4-oxadiazole 
• 52770-91-9 3-(acetylamino)-5-phenyl-1,2,4-oxadiazole 
• 830-03-5 4-nitrophenol acetate 
• 108-24-7 acetic anhydride 
• 1612-76-6 2-amino-5-phenyl-1,3,4-oxadiazole 
• 613-94-5 benzoic acid hydrazide 
• 506-96-7 Acetyl bromide 
• 75-36-5 acetyl chloride 

Downstream Products

• 65551-62-4 N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-glycine 
• 65929-57-9 1-acetoxy-1-phenyl-2-(5-phenyl-[1,3,4]oxadiazol-2-ylamino)-ethane 
• 65551-64-6 1-phenyl-2-(5-phenyl-[1,3,4]oxadiazol-2-ylamino)-ethanol 
• 14632-22-5 N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-acetamide; sodium salt 
• 65551-63-5 N-(2-oxo-2-phenyl-ethyl)-N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-acetamide 
• 36944-02-2 N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-glycine ethyl ester 
• 7658-76-6 3-acetyl-2-acetylimino-5-phenyl-2,3-dihydro-[1,3,4]oxadiazole 

Relevant articles and documents

Experimental and DFT studies on competitive heterocyclic rearrangements. Part 2: A one-atom side-chain versus the classic three-atom side-chain (Boulton-Katritzky) ring rearrangement of 3-acylamino-1,2,4-oxadiazoles

(Chemical Equation Presented) The experimental investigation of the base-catalyzed rearrangements of 3-acylamino-1,2,4-oxadiazoles evidenced a new reaction pathway which competes with the well-known ring-degenerate Boulton-Katritzky rearrangement (BKR). T

Influence of solvent from which crystals of 2-amino-5-aryl-1,3,4-oxadiazoles grow on acetylation reaction in solid state

The phenomenon of reaction anisotropy, i.e. forming of different products on different crystals' facets, is characteristic for 2-amino-5-aryl-1,3,4-oxadiazoles solid-state acetylation. In this case, the ratio of products in reaction yield depends on the f

Reaktionen N-metallierter 2-Amino-5-aryl-1,3,4-oxadiazole

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