2425-95-8|2,5-Bis(4-aminophenyl)-1,3,4-oxadiazole

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2,5-Bis(4-aminophenyl)-1,3,4-oxadiazole | CAS:2425-95-8

2,5-Bis(4-aminophenyl)-1,3,4-oxadiazole

Name：2,5-Bis(4-aminophenyl)-1,3,4-oxadiazole
CAS：2425-95-8
Synonyms：4,4'-(1,3,4-Oxadiazole-2,5-diyl)dianiline
Molecular Formula：C₁₄H₁₂N₄O
Molecular Weight：252.27
EINESC：219-373-8

Description

Properties

Melting point	252-255 ºC

Safety

Symbol(GHS)	Xi
Hazard Codes	R36/37/38
SDS/MSDS	S26;S37/39

SDS

Source	SDS/MSDS Samples
Sigma-Aldrich	View & Download

Synthetic Route

Name	CAS

Articles

Peer-Reviewed Papers

(Bmim) Br3 as a New Reagent for Regioselective Monobromination of Phenols and Several Activated Aromatics under Solvent-free Conditions. Le ZG, et al. Chin. J. Chem., 23(11), 1537-1540 (2005) Synthesis of aromatic bisabolene natural products via palladium-catalyzed cross-couplings of organozinc reagents.James R Vyvyan et al.The Journal of organic chemistry, 69(7), 2461-2468 (2004-03-31) Electrophilic Aromatic Bromination Using Bromodimethylsulfonium Bromide Generated in Situ.George Majetich et al.The Journal of organic chemistry, 62(13), 4321-4326 (1997-06-27) The isopropyl cresols. Carpenter MS and Easter WM. The Journal of Organic Chemistry, 20(4), 401-411 (1955) Total synthesis of (?)-heliannuol D, an allelochemical from Helianthus annuus.Vyvyan JR and Looper RE. Tetrahedron Letters, 41(8), 1151-1154 (2000) A useful Pd-catalyzed Negishi coupling approach to benzylic sulfonamide derivatives.Gang Zhou et al.Organic letters, 10(12), 2517-2520 (2008-05-22)

Remarks

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Name	CAS

Description

Properties

Safety

SDS

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