90004-05-0

Basic information

• Product Name: 2-(1,3,4-oxadiazol-2-yl)aniline(SALTDATA: FREE)
• Synonyms: 2-(1,3,4-oxadiazol-2-yl)aniline(SALTDATA: FREE);2-[1,3,4]Oxadiazol-2-yl-phenylamine
• CAS NO: 90004-05-0
• Molecular Formula: C₈H₇N₃O
• Molecular Weight: 161.16068
• Mol File: 90004-05-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(1,3,4-oxadiazol-2-yl)aniline(SALTDATA: FREE)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1,3,4-oxadiazol-2-yl)aniline(SALTDATA: FREE)(90004-05-0)
• EPA Substance Registry System: 2-(1,3,4-oxadiazol-2-yl)aniline(SALTDATA: FREE)(90004-05-0)

Safety Data

• Hazardous Substances Data: 90004-05-0(Hazardous Substances Data)

Usage

Uses

2-[1,3,4]Oxadiazol-2-yl-phenylamine is used in preparation of Heteroaryl compounds as ZNF143 inhibitors.

Upstream product

• 89898-92-0 2-(2-nitrophenyl)-1,3,4-oxadiazole 
• 96239-47-3 1-(2-Aminobenzoyl)-2-dimethylaminomethylene Hydrazine 
• 122-51-0 orthoformic acid triethyl ester 
• 1904-58-1 anthranilic acid hydrazide 
• 57711-25-8 3,4-Dihydro-5H-1,3,4-benzotriazepin-5-one 
• 606-26-8 o-nitrobenzohydrazide 
• 118-92-3 anthranilic acid 
• 73789-56-7 N-isocyaniminotriphenylphosphorane 

Relevant articles and documents

Synthesis and single crystal X-ray structure of 2-(1,3,4-oxadiazol-2-yl) aniline

Reaction of 2-aminobenzoic acid with (N-isocyanimino)triphenylphosphorane proceeds smoothly at r. t. to afford 2-(1,3,4-oxadiazol-2-yl)aniline in high yield. The structure of this compound was confirmed by IR, 1H, and 13C NMR spectro

Novel, fast and efficient one-pot sonochemical synthesis of 2-aryl-1,3,4-oxadiazoles

Ultrasound promoted synthesis of 2-aryl-1,3,4-oxadiazoles at ambient temperature is reported. The remarkable features of the new procedure are shorter reaction time, excellent yields, cleaner reaction profile and simple experimental and workup procedure.

1,3,4-Benzotriazepinones. Formation and rearrangement

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