1,3-Bis(di-i-propylphosphino)propane, min. 98% (dippp)|15-0680|91159-11-4

1,3-Bis(di-i-propylphosphino)propane, min. 98% (dippp)

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Sku SC15-0680_100_MG
US-Strem
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Product Information

Product Name
1,3-Bis(di-i-propylphosphino)propane, min. 98% (dippp)
Brand Name
US-Strem
Product Number
15-0680
CAS
91159-11-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
534190
IUPAC Name
3-di(propan-2-yl)phosphanylpropyl-di(propan-2-yl)phosphane
InChI Key
QRPNDOFSVHOGCK-UHFFFAOYSA-N
SMILES
CC(C)P(CCCP(C(C)C)C(C)C)C(C)C

Application

Technical Notes:
1. Catalyst for the cross-methylation of aryl chlorides using stabilized dimethylaluminum or dimethylgallium reagents .
2.Catalyst used in base-free olefin arylation.
3.Catalyst for the efficient carbonylation of aryl chlorides.
References:
1.Synthesis, 2000, 4, 571.
2.Organometallics, 1993, 12, 4734.
3. J. Am. Chem. Soc., 1989, 111, 8742.
4. J. Chem. Soc. Chem. Comm., 1989, 1816.

References Data Source From Pubchem

Controlled/Living Polymerization Toward Conjugated Polymers
Publication Name: Springer Handbook of Functional Polymers
Publication Date: 2025
DOI: 10.1007/978-981-96-2498-0_10

Chalcogenide Cluster Complexes of Group Five Transition Metals: Synthetic and Structural Aspects
Publication Name: Journal of Structural Chemistry
Publication Date: 2019-10
DOI: 10.1134/s0022476619100019

Nitrosyl Complexes in Homogeneous Catalysis
Publication Name: Nitrosyl Complexes in Inorganic Chemistry, Biochemistry and Medicine I
Publication Date: 2013
DOI: 10.1007/430_2013_97

Synthesis from Bis(halophosphino)alkanes and Organometallic Compounds
Publication Name: Science of Synthesis
Publication Date: 2009

Reductive Carbonylation of Haloarenes and Related Compounds Using Carbon Monoxide
Publication Name: Science of Synthesis
Publication Date: 2007