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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)-

4-Eicosene-1,3-diol, 2-amino-, (2S,3R,4E)-

CCCCCCCCCCCCCCC/C=C/[C@H]([C@H](CO)N)O Request for Quotation
Chemical Name: 4-Eicosene-1,3-diol, 2-amino-, (2S,3R,4E)-
CAS Number: 6918-49-6
Product Number: AG00FBIS(AGN-PC-0OGPWN)
Synonyms:
MDL No:
Molecular Formula: C20H41NO2
Molecular Weight: 327.5450

Identification/Properties

Computed Properties
Molecular Weight:
327.553g/mol
XLogP3:
6.4
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
17
Exact Mass:
327.314g/mol
Monoisotopic Mass:
327.314g/mol
Topological Polar Surface Area:
66.5A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
256
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


C20-Sphingosine is a versatile compound that finds wide application in chemical synthesis. It is commonly used in the production of novel lipids, particularly in the context of lipidomics research and drug development. Due to its unique structure and properties, C20-Sphingosine serves as a valuable building block for the synthesis of sphingolipids, which play crucial roles in various cellular functions.In chemical synthesis, C20-Sphingosine can be incorporated into the molecular structure of lipids to modify their biological activities or to create tailored lipid derivatives with specific properties. Researchers often utilize C20-Sphingosine as a key intermediate in the design and synthesis of bioactive compounds for studying signaling pathways and lipid metabolism. Its ability to mimic natural lipids makes it an essential tool for investigating the structure-function relationships of complex lipid molecules.Furthermore, C20-Sphingosine's involvement in chemical synthesis extends to the development of pharmaceuticals and cosmetics. By incorporating this compound into the formulation of drugs or skincare products, researchers can enhance their efficacy and bioavailability. Its compatibility with biological systems and potential therapeutic benefits make C20-Sphingosine a valuable asset in pharmaceutical research and development.Overall, the application of C20-Sphingosine in chemical synthesis offers a promising avenue for creating innovative lipid-based molecules with diverse functionalities and applications in various scientific disciplines.