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Copper (I) diphenylphosphinate

Catalog Number
ACM1011257423
Product Name
Copper (I) diphenylphosphinate
Structure
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CAS
1011257-42-3
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Synonyms
SCHEMBL1333677; Copper (I) diphenylphosphinate; TC-068616; MFCD09702021; AKOS015840647; Phosphinic acid, P,P-diphenyl-, copper(1+) salt (1:1); $l^{1}-copper(1+) ion diphenylphosphinate; 1011257-42-3; FT-0685402; Y6783;
IUPAC Name
copper(1+);diphenylphosphinate;
Molecular Weight
280.73g/mol
Molecular Formula
C12H10CuO2P;
Canonical SMILES
C1=CC=C(C=C1)P(=O)(C2=CC=CC=C2)[O-].[Cu+];
InChI
InChI=1S/C12H11O2P.Cu/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12;/h1-10H,(H,13,14);/q;+1/p-1;
InChI Key
SVIKVYNAINDOJS-UHFFFAOYSA-M;
Complexity
210
Covalently-Bonded Unit Count
2
Exact Mass
279.971g/mol
H-Bond Acceptor
2
Heavy Atom Count
16
Monoisotopic Mass
279.971g/mol
Rotatable Bond Count
2
Topological Polar Surface Area
40.1A^2
Application
Copper (I) diphenylphosphinate serves as a catalyst in the enantioselective synthesis of (-)-viridin and (-)-viridiol, which are fungal steroids with phytotoxic activity. Additionally, it plays a crucial role in the stereoselective synthesis of the C1-C16 fragment of goniodomin A.
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