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((2,4,6-Tri-isopropyl)phenyl)di-cyclohexylphosphine

Catalog Number
ACM303111968
Product Name
((2,4,6-Tri-isopropyl)phenyl)di-cyclohexylphosphine
Structure
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CAS
303111-96-8
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Synonyms
Dicyclohexyl[2,4,6-Tris(1-Methylethyl)Phenyl]Phosphine
IUPAC Name
dicyclohexyl-[2,4,6-tri(propan-2-yl)phenyl]phosphane
Molecular Weight
400.62
Molecular Formula
C27H45P
Canonical SMILES
CC(C)C1=CC(=C(C(=C1)C(C)C)P(C2CCCCC2)C3CCCCC3)C(C)C;
InChI
DTSPXGRQYHLKLO-UHFFFAOYSA-N
InChI Key
InChI=1S/C27H45P/c1-19(2)22-17-25(20(3)4)27(26(18-22)21(5)6)28(23-13-9-7-10-14-23)24-15-11-8-12-16-24/h17-21,23-24H,7-16H2,1-6H3
Boiling Point
479.5±44.0 °C(Predicted)
Melting Point
138-140 °C
Purity
98%
Appearance
Solid
Complexity
405
Covalently-Bonded Unit Count
1
Exact Mass
400.326g/mol
Heavy Atom Count
28
Isomeric SMILES
CC(C)C1=CC(=C(C(=C1)C(C)C)P(C2CCCCC2)C3CCCCC3)C(C)C
Monoisotopic Mass
400.326g/mol
Rotatable Bond Count
6
Topological Polar Surface Area
0A^2
Application
The purpose of ((2,4,6-Tri-isopropyl)phenyl)di-cyclohexylphosphine is to serve as a versatile catalyst, facilitating key chemical transformations. It is effectively used in the Suzuki reaction, an essential process in organic synthesis for forming carbon-carbon bonds. Additionally, this product acts as a catalyst in the oxidation of alcohols, transforming them into aldehydes or ketones, and plays a critical role in the hydrodechlorination of chloroarenes, converting them into less toxic, more reactive compounds. Its multifunctional capabilities make it an invaluable tool for various industrial and research applications.
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