TrixiePhos

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Catalog Number
ACM255836670
Product Name
TrixiePhos
Structure
Structure
CAS
255836-67-0
Category
Organic Phosphine Compounds
Synonyms
racemic 2-(di-tert-butylphosphino)-1,1'-binaphthyl; RACEMIC-2-DI-TERT-BUTYLPHOSPHINO-1,1-BINAPHTHYL; 1,1'-binaphthyl-2-yl di-tert-butylphosphine; racemic 2-di-tert-butylphosphino-1,1'-binaphthyl; AK-48836; AX8150194; 2-(di-ter-butylphosphino)-1,1'-binaphthyl; 2-(DI-TERT-BUTYLPHOSPHINO)-1,1-BINAPHTHYL; 2-(di-t-butylphosphino)-1,1'-binaphtyl; 2-(di-tert-butylphosphino)-1,1'-binapthyl;
IUPAC Name
ditert-butyl-(1-naphthalen-1-ylnaphthalen-2-yl)phosphane;
Molecular Weight
398.53g/mol
Molecular Formula
C28H31P;
Canonical SMILES
CC(C)(C)P(C1=C(C2=CC=CC=C2C=C1)C3=CC=CC4=CC=CC=C43)C(C)(C)C;
InChI
InChI=1S/C28H31P/c1-27(2,3)29(28(4,5)6)25-19-18-21-13-8-10-16-23(21)26(25)24-17-11-14-20-12-7-9-15-22(20)24/h7-19H,1-6H3;
InChI Key
QGBQGMHXBSLYLZ-UHFFFAOYSA-N;
Application
Ligand for the Pd-catalyzed formation of oxygen heterocycles.

Ligand for the intermolecular Pd-catalyzed synthesis of aryl ethers.

Ligand for the intramolecular Pd-catalyzed synthesis of aryl ethers.

Ligand for the synthesis of carbazoles by Pd-catalyzed double N-arylation reaction.

Ligand for the Pd-catalyzed cyanation of (hetero)arylchlorides.

Ligand for the Pd-catalyzed intramolecular synthesis of carbazoles via C-H functionalization.
Complexity
524
Covalently-Bonded Unit Count
1
Exact Mass
398.216g/mol
Heavy Atom Count
29
Monoisotopic Mass
398.216g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
0A^2
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