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  2. 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-bis[2,4-bis(1,1-dimethylethyl)phenoxy]-

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-bis[2,4-bis(1,1-dimethylethyl)phenoxy]-

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Chemical Name: 2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-bis[2,4-bis(1,1-dimethylethyl)phenoxy]-
CAS Number: 26741-53-7
Product Number: AG00ILNB(AGN-PC-0R2ONM)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
604.705g/mol
XLogP3:
9.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
604.308g/mol
Monoisotopic Mass:
604.308g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
41
Formal Charge:
0
Complexity:
764
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,9-Bis(2,4-di-tert-butylphenoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane, utilized in chemical synthesis, acts as a versatile building block in the creation of novel organic compounds and materials. This compound is particularly valuable in the formation of complex molecular structures due to its unique spirocyclic framework and the presence of phosphorus atoms, which can serve as key binding sites for further functionalization reactions. Its highly sterically hindered tert-butylphenoxy groups provide steric protection and enhance the compound's stability during various synthetic transformations. The spirocyclic nature of this molecule also imparts rigidity and structural integrity, making it an ideal scaffold for constructing intricate molecular architectures with defined spatial arrangements. In chemical synthesis, this compound serves as a crucial component for designing and developing advanced materials, pharmaceuticals, and specialty chemicals with tailored properties and functionalities.