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Bis(3,5-dimethyl-4-methoxyphenyl)chlorophosphine
PRICE INQUIRYCatalog Number
ACM136802852-2
Product Name
Bis(3,5-dimethyl-4-methoxyphenyl)chlorophosphine
Structure
![{[CurrentData.Name]}](https://resource.alfachemic.com/structure/136802-85-2.gif)
CAS
136802-85-2
Synonyms
RT-011532; AKOS015910269; J-006913; DB-009591; FT-0770222; Phosphinous chloride,P,P-bis(4-methoxy-3,5-dimethylphenyl)-; BIS(3,5-DIMETHYL-4-METHOXYPHENYL)CHLOROPHOSPHINE; chlorobis(4-methoxy-3,5-dimethylphenyl)phosphine; ZINC100100721; 136802-85-2;
IUPAC Name
chloro-bis(4-methoxy-3,5-dimethylphenyl)phosphane;
Molecular Weight
336.796g/mol
Molecular Formula
C18H22ClO2P;
Canonical SMILES
CC1=CC(=CC(=C1OC)C)P(C2=CC(=C(C(=C2)C)OC)C)Cl;
InChI
InChI=1S/C18H22ClO2P/c1-11-7-15(8-12(2)17(11)20-5)22(19)16-9-13(3)18(21-6)14(4)10-16/h7-10H,1-6H3;
InChI Key
JWCZKGYRAINWJA-UHFFFAOYSA-N;
Complexity
298
Covalently-Bonded Unit Count
1
Exact Mass
336.105g/mol
H-Bond Acceptor
2
Heavy Atom Count
22
Monoisotopic Mass
336.105g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
18.5A^2
Application
Bis(3,5-dimethyl-4-methoxyphenyl)chlorophosphine serves a critical role in advancing the field of asymmetric synthesis and catalysis. It is utilized as a reactant in a variety of chemical processes, such as asymmetric organocatalytic electrophilic phosphination and asymmetric hydroformylation using Taddol-based chiral phosphine-phosphite ligands. Additionally, it is instrumental in the synthesis of ferrocene-based chiral diphosphines and plays a part in the alcoholysis of phosphane-boranes. Moreover, this compound is used in asymmetric hydrogenations of bifep-type biferrocenes, underscoring its versatility and significance in the development of chiral molecules essential for various chemical applications.
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