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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)-

N,N,2,6-Tetramethyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine

CN(p1oc2c(C)cc3c(c2c2c(o1)c(C)cc1c2cccc1)cccc3)C Request for Quotation
Chemical Name: N,N,2,6-Tetramethyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
CAS Number: 185449-86-9
Product Number: AG00AB1Z(AGN-PC-009E1Q)
Synonyms:
MDL No:
Molecular Formula: C24H42NO2P
Molecular Weight: 407.5695

Identification/Properties

Computed Properties
Molecular Weight:
387.419g/mol
XLogP3:
6.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
387.139g/mol
Monoisotopic Mass:
387.139g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
513
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (11bS)-N,N,2,6-Tetramethyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine plays a pivotal role in chemical synthesis as a versatile building block and reagent. Its unique structure and properties make it an invaluable tool in the creation of complex organic molecules and materials. When used in chemical synthesis, this compound can act as a chiral catalyst, enabling the selective formation of specific enantiomers in asymmetric reactions. Additionally, its phosphorus-containing moiety can serve as a key functional group for further derivatization, allowing for the modification of its chemical properties and reactivity. Furthermore, the presence of the dioxaphosphepin ring system provides a scaffold for the construction of elaborate molecular architectures through various bond-forming reactions. This compound's ability to participate in a wide range of chemical transformations makes it a valuable asset in the toolkit of synthetic chemists seeking to access novel compounds for pharmaceuticals, materials science, and other applications.