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5-(Di-tert-butylphosphino)-1-(naphthalen-1-yl)-1H-pyrazole

Catalog Number
ACM894085973-1
Product Name
5-(Di-tert-butylphosphino)-1-(naphthalen-1-yl)-1H-pyrazole
CAS
894085-97-3
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Synonyms
5-(Di-tert-butylphosphanyl)-1-(naphthalen-1-yl)-1H-pyrazole; ACMC-20am7s; ditert-butyl-(2-naphthalen-1-ylpyrazol-3-yl)phosphane; DB-009554; AKOS025394903; 894085-97-3; CTK5G3073; 5-[BIS(TERT-BUTYL)PHOSPHINO]-1-(1-NAPHTHALENYL)-1H-PYRAZOLE; ZINC44831022; 5-(Di-t-butylphosphino)-1-(naphthalen-1-yl)-1H-pyrazole;
IUPAC Name
ditert-butyl-(2-naphthalen-1-ylpyrazol-3-yl)phosphane;
Molecular Weight
338.435g/mol
Molecular Formula
C21H27N2P;
Canonical SMILES
CC(C)(C)P(C1=CC=NN1C2=CC=CC3=CC=CC=C32)C(C)(C)C;
InChI
InChI=1S/C21H27N2P/c1-20(2,3)24(21(4,5)6)19-14-15-22-23(19)18-13-9-11-16-10-7-8-12-17(16)18/h7-15H,1-6H3;
InChI Key
XJZYJFVKLNCBQF-UHFFFAOYSA-N;
Complexity
409
Covalently-Bonded Unit Count
1
Exact Mass
338.191g/mol
H-Bond Acceptor
1
Heavy Atom Count
24
Monoisotopic Mass
338.191g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
17.8A^2
Application
The purpose of 5-(Di-tert-butylphosphino)-1-(naphthalen-1-yl)-1H-pyrazole is to serve as an effective catalyst in amination reactions. This compound facilitates the formation of amine bonds by enhancing the efficiency and selectivity of the reaction process, ultimately leading to improved yields and reduced reaction times. Its unique structure allows it to stabilize transition states and lower activation energies, making it an invaluable component in synthetic chemistry applications where precision and efficacy are paramount.
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