[4-(N,N-Dimethylamino)phenyl]di-t-butylphosphine, min. 95% amphos|15-1248|932710-63-9

[4-(N,N-Dimethylamino)phenyl]di-t-butylphosphine, min. 95% amphos

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Sku SC15-1248_25_G
US-Strem
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Product Information

Product Name
4-(N,N-Dimethylamino)phenyldi-t-butylphosphine, min. 95% amphos
Brand Name
US-Strem
Product Number
15-1248
CAS
932710-63-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11714598
IUPAC Name
4-ditert-butylphosphanyl-N,N-dimethylaniline
InChI Key
IQTHEAQKKVAXGV-UHFFFAOYSA-N
SMILES
CC(C)(C)P(C1=CC=C(C=C1)N(C)C)C(C)(C)C

Application

Technical Notes:
1. Ligand used in a highly-active palladium precatalyst for the efficient amination of aryl chloride. 2. Ligand used in the palladium-catalyzed annulations under microwave enhanced conditions.
References:
1.Organometallics, 2011, 30, 4432.
2. Tetrahedron Letters, 2013, 54, 5126.

References Data Source From Pubchem

Evolution of catalyst transfer polymerization toward complex conjugated polymer architectures
Publication Name: Polymer Journal
Publication Date: 2026-02-19
DOI: 10.1038/s41428-026-01146-9

On-DNA C–H functionalization of electron-rich arenes for DNA-encoded libraries
Publication Name: Nature Chemistry
Publication Date: 2025-06-16
DOI: 10.1038/s41557-025-01844-6

Anwendung von Organometallkatalysatoren in der API-Synthese
Publication Name: Organometallik in der Prozesschemie
Publication Date: 2024
DOI: 10.1007/978-3-031-52858-3_4

Synthesis of Navoximod
Publication Name: Synfacts
Publication Date: 2022-07-18
DOI: 10.1055/s-0041-1738225

Recent Advances in Thianthrenation/Phenoxathiination Enabled Site-Selective Functionalization of Arenes
Publication Name: Synthesis
Publication Date: 2022-06-28
DOI: 10.1055/s-0041-1737493