ChemicalBook--->CAS DataBase List--->380230-02-4

380230-02-4

380230-02-4 Structure

380230-02-4 Structure
IdentificationBack Directory
[Name]

(+)-N,N-BIS[(1S)-1-PHENYLETHYL]-DINAPHTHO[2,1-D:1',2'-F][1,3,2]DIOXAPHOSPHEPIN-4-AMINE, (11BR)
[CAS]

380230-02-4
[Synonyms]

3,4-a'
(S,S,S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHE
]dinaphthalen-4-yl)bis(1-phenylethyl)amine
]dinaphthalen-4-yl)bis[(1S)-1-phenylethyl]amine.
3,4-a']dinaphthalen-4-yl)bis[(1S)-1-phenylethyl]amine
3,4-a']dinaphthalen-4-yl)bis[(1S)-1-phenylethyl]amine,95%
(S,S,S)-(+)-(3,5-Dioxa-4-phosphacyclohepta[2,1-a:3,4-a’
3,4-a']dinaphthalen-4-yl)bis[(1S)-1-phenylethyl]amine,min.95%
3,4-a']dinaphthalen-4-yl)bis[(1S)-1-phenylethyl]amine, min. 95%
N,N-Bis((S)-1-phenylethyl)dinaphtho-[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
N,N-Bis[(1S)-1-phenylethyl]-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
(+)-N,N-BIS[(1S)-1-PHENYLETHYL]-DINAPHTHO[2,1-D:1',2'-F][1,3,2]DIOXAPHOSPHEPIN-4-AMINE, (11BR)
(S,S,S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHEPTA[2,1-A:3,4-A']DINAPHTHALEN-4-YL)BIS(1-PHENYLETHYL)AMINE
(S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHEPTA[2,1-A:3,4-A']DINAPHTHALEN-4-YL)BIS[(1S)-1-PHENYLETHYL]AMINE
(S,S,S)-(+)-(3,5-Dioxa-4-phosphacyclohepta[2,1-a:3,4-a']dinaphthalen-4-yl)bis(1-phenylethyl)aMine 97%
S)-(+)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a:3,4-a']dinaphthalen-4-yl)bis[(1S)-1-phenylethyl]amine,min.95%
(S)-(+)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a:3,4-a']dinaphthalen-4-yl)bis[(1S)-1-phenylethyl]amine, min. 95%
[Molecular Formula]

C36H30NO2P
[MDL Number]

MFCD04117688
[MOL File]

380230-02-4.mol
[Molecular Weight]

539.6
Chemical PropertiesBack Directory
[Melting point ]

88-89 °C
[alpha ]

+13.1° (c 1.01, CHCl3)
[form ]

Powder
[color ]

off-white
[Sensitive ]

moisture sensitive
Safety DataBack Directory
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[WGK Germany ]

3
Questions And AnswerBack Directory
[Reaction]

  1. A ligand for asymmetric conjugate addition of dialkyl zinc reagents to activated olefins.
  2. Iridium-catalyzed regioselective and enantioselective allylation of enamines.
  3. Iridium-catalyzed asymmetric allylation of KSAc. 
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