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2-[2-(Dicyclohexylphosphino)phenyl]-N-methylindole

Catalog Number
ACM1067883582-1
Product Name
2-[2-(Dicyclohexylphosphino)phenyl]-N-methylindole
Structure
2-[2-(Dicyclohexylphosphino)phenyl]-N-methylindole
CAS
1067883-58-2
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Synonyms
2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole; CM-Phos
IUPAC Name
dicyclohexyl-[2-(1-methylindol-2-yl)phenyl]phosphane
Molecular Weight
403.54
Molecular Formula
C27H34NP
InChI
PFJAHDIIEPTASS-UHFFFAOYSA-N
InChI Key
InChI=1S/C27H34NP/c1-28-25-18-10-8-12-21(25)20-26(28)24-17-9-11-19-27(24)29(22-13-4-2-5-14-22)23-15-6-3-7-16-23/h8-12,17-20,22-23H,2-7,13-16H2,1H3
Boiling Point
582.4±33.0 °C(Predicted)
Melting Point
180-185 °C
Purity
97%
Appearance
Solid
Complexity
491
Covalently-Bonded Unit Count
1
Exact Mass
403.243g/mol
Heavy Atom Count
29
Isomeric SMILES
CN1C2=CC=CC=C2C=C1C3=CC=CC=C3P(C4CCCCC4)C5CCCCC5
Monoisotopic Mass
403.243g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
4.9A^2
Application
Suzuki-Miyaura Coupling of Aryl Mesylates and alkenyl tosylate and mesylate bearing alkyl, methoxy, aldehyde, keto, nitrile, ester, and heteroaryl substitution.

Sonogashira Coupling of Aryl Mesylates, R' = alkyl, aryl; R = C(O)R, COOMe, CHO, CN.

Buchwald-Hartwig Amination of Aryl Mesylates, R = cyano, chloro, methoxy, keto, ester and etc.

Additional catalyzed reactions include Cyanation of functional Aryl Mesylates and Chlorides; Hiyama Coupling of Aryl Mesylates; Direct Arylation of Heterocycles with Aryl Mesylates; Borylation of Aryl Mesylates.
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