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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-[[2-(hexadecanoylamino)-4-nitrophenoxy]-hydroxyphosphoryl]oxyethyl-trimethylazanium;hydroxide

CCCCCCCCCCCCCCCC(=O)Nc1cc(ccc1OP(=O)(OCC[N+](C)(C)C)O)[N+](=O)[O-].[OH-] Request for Quotation
Chemical Name: 2-[[2-(hexadecanoylamino)-4-nitrophenoxy]-hydroxyphosphoryl]oxyethyl-trimethylazanium;hydroxide
CAS Number: 60438-73-5
Product Number: AG00EC0M(AGN-PC-0JPT3E)
Synonyms:
MDL No:
Molecular Formula: C27H50N3O8P
Molecular Weight: 575.674961

Identification/Properties

Properties
MP:
165-169°C (dec.)
Storage:
-10 ℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
575.684g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
21
Exact Mass:
575.334g/mol
Monoisotopic Mass:
575.334g/mol
Topological Polar Surface Area:
132A^2
Heavy Atom Count:
39
Formal Charge:
0
Complexity:
712
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2-(N-Hexadecanoylamino)-4-nitrophenylphosphocholine hydroxide is a versatile molecule commonly utilized in chemical synthesis processes. This unique compound serves as a crucial building block in the creation of various phospholipids and phosphocholine derivatives. Its ability to selectively modify specific functional groups makes it an essential tool in the development of novel pharmaceuticals and bioactive molecules. Additionally, its amphiphilic nature allows for the precise manipulation of membrane structures, making it a valuable component in lipid bilayer studies and drug delivery systems. In chemical synthesis, this compound plays a pivotal role in facilitating complex reactions and enabling the synthesis of highly specialized phospholipid analogs with tailored properties for a wide range of applications in research and industry.