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33989-10-5

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33989-10-5 Structure

33989-10-5 Structure
IdentificationBack Directory
[Name]

(1,10-PHENANTHROLINE)BIS(TRIPHENYLPHOSPHINE)COPPER (I) NITRATE DICHLOROMETHANE ADDUCT
[CAS]

33989-10-5
[Synonyms]

(1,10-Phenanthroline)bis(triphenylphosphine)copper nitrate
copper(1+):dichloromethane:1,10-phenanthroline:triphenylphosphane:nitrate
(1,10-PHENANTHROLINE)BIS(TRIPHENYLPHOSPHINE)COPPER (I) NITRATE DICHLOROMETHANE ADDUCT
(1,10-Phenanthroline)bis(triphenylphosphine)copper(I)nitratedichloromethaneadduct,98%
(1,10-Phenanthroline)bis(triphenylphosphine)copper(I) nitrate dichloromethane adduct 95%
[Molecular Formula]

C49H40Cl2CuN3O3P2
[MDL Number]

MFCD07369033
[MOL File]

33989-10-5.mol
[Molecular Weight]

915.26
Chemical PropertiesBack Directory
[Melting point ]

202-204°C
[storage temp. ]

2-8°C, protect from light, stored under nitrogen
[form ]

Powder
[color ]

yellow
[InChIKey]

JPYCIEWKXHWRBU-UHFFFAOYSA-N
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39-36
[WGK Germany ]

2
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Questions And AnswerBack Directory
[Reaction]

  1. High yield synthesis of 2-arylbenzo[b]furans via the copper (I) catalyzed coupling of o-iodophenols and aryl acetylenes.
  2. High yield synthesis of vinyl sulfides.
  3. Efficient synthesis of 1,3-enynes.
  4. Effective synthesis of 2-substituted indoles.
  5. Synthesis of 1,4-disubstituted 5-iodotriazoles.
  6. Selective cyclization strategy to 2-substitued benzofurans and indoles.
  7. Copper-catalyzed cascade reaction to 2-indolyl-C-glycosides.
Reactions of 33989-10-5
Hazard InformationBack Directory
[reaction suitability]

core: copper
reagent type: catalyst
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