1,3-BIS(2,6-DIISOPROPYLPHENYL)-IMIDAZOLIDINIUM-CHLORIDE

Modify Date: 2024-01-02 10:55:51

1,3-BIS(2,6-DIISOPROPYLPHENYL)-IMIDAZOLIDINIUM-CHLORIDE structure	Common Name	1,3-BIS(2,6-DIISOPROPYLPHENYL)-IMIDAZOLIDINIUM-CHLORIDE
	CAS Number	258278-25-0	Molecular Weight	427.065
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₂₇H₃₉ClN₂	Melting Point	289-293ºC(lit.)
	MSDS	Chinese USA	Flash Point	N/A
	Symbol	GHS07	Signal Word	Warning

Name	1,3-bis(2,6-diisopropylphenyl)-imidazolidinium-chloride
Synonym	More Synonyms

Melting Point	289-293ºC(lit.)
Molecular Formula	C₂₇H₃₉ClN₂
Molecular Weight	427.065
Exact Mass	426.280182
PSA	6.25000
LogP	7.39650

MSDS(Chinese)

Symbol	GHS07
Signal Word	Warning
Hazard Statements	H315-H319-H335
Precautionary Statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes	Xi: Irritant;
Risk Phrases	R36/37/38
Safety Phrases	S26
RIDADR	NONH for all modes of transport

Palladium-(N-heterocyclic carbene) hydrogenation catalysts.

Angew. Chem. Int. Ed. Engl. 44 , 2026, (2005)

NHC-catalyzed ring expansion of oxacycloalkane-2-carboxaldehydes: a versatile synthesis of lactones.

Org. Lett. 11 , 891, (2009)

Imidazolinium-derived carbenes catalyze the ring-expansion lactonization of oxacycloalkane-2-carboxaldehydes. A variety of functionalized five-, six-, and seven-membered lactones can be formed efficie...

Palladium-imidazolium carbene catalyzed Mizoroki-Heck coupling with aryl diazonium ions.

J. Org. Chem. 4 , 2079, (2002)

[reaction: see text] Catalyst formed from N,N-bis(2,6-diisopropylphenyl)dihydroimidazolium chloride and palladium(II) acetate (2 mol %) was used, without added base, to efficiently produce Heck couple...

SIPr.HCl

MFCD07369796

1H-Imidazolium, 1,3-bis[2,6-bis(1-methylethyl)phenyl]-4,5-dihydro-, chloride (1:1)

1,3-Bis(2,6-diisopropylphenyl)iMidazoliniuM Chloride

1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydro-1H-imidazol-3-ium chloride

1,3-Bis(2,6-diisopropylphenyl)imidazolidinium chloride