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  2. 1,3,2-Dioxaphosphorinane, 4-(2-chlorophenyl)-2-hydroxy-5,5-dimethyl-,2-oxide, (4S)-

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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)-

1,3,2-Dioxaphosphorinane, 4-(2-chlorophenyl)-2-hydroxy-5,5-dimethyl-,2-oxide, (4S)-

Clc1ccccc1[C@H]1OP(=O)(O)OCC1(C)C Request for Quotation
Chemical Name: 1,3,2-Dioxaphosphorinane, 4-(2-chlorophenyl)-2-hydroxy-5,5-dimethyl-,2-oxide, (4S)-
CAS Number: 98674-86-3
Product Number: AG003CE4(AGN-PC-0W8IK4)
Synonyms:
MDL No:
Molecular Formula: C11H14ClO4P
Molecular Weight: 276.6532

Identification/Properties

Properties
MP:
228-234°C(lit.)
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
276.653g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
276.032g/mol
Monoisotopic Mass:
276.032g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
333
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, (4S)-4-(2-Chlorophenyl)-2-hydroxy-5,5-dimethyl-1,3,2-dioxaphosphinane 2-oxide, often referred to simply as $name$, serves as a versatile building block for creating complex organic molecules. This compound's unique structure, featuring a phosphorus atom in a cyclic dioxaphosphinane ring, imparts distinctive reactivity and functional group compatibility, making it a valuable tool in organic synthesis. One key application of $name$ is in the formation of phosphorus-containing ligands for catalytic processes. By modifying the hydroxyl and chlorophenyl groups on the phosphorus atom, chemists can tailor the ligand's steric and electronic properties to enhance its coordination with metal catalysts. This, in turn, enables the selective activation of specific bonds in target molecules, facilitating the synthesis of intricate organic compounds with high efficiency and selectivity.