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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)-

9-Octadecenoic acid (9Z)-, (2S)-2-(acetyloxy)-3-hydroxypropyl ester

CCCCCCCCC=CCCCCCCCC(=O)OC[C@@H](OC(=O)C)CO Request for Quotation
Chemical Name: 9-Octadecenoic acid (9Z)-, (2S)-2-(acetyloxy)-3-hydroxypropyl ester
CAS Number: 86390-77-4
Product Number: AG004XD8(AGN-PC-0V4R52)
Synonyms:
MDL No:
Molecular Formula: C23H42O5
Molecular Weight: 398.5766

Identification/Properties

Properties
Storage:
Keep in dry area;-10 ℃;Inert atmosphere;
Computed Properties
Molecular Weight:
398.584g/mol
XLogP3:
6.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
21
Exact Mass:
398.303g/mol
Monoisotopic Mass:
398.303g/mol
Topological Polar Surface Area:
72.8A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
406
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


1-Oleoyl-2-acetyl-sn-glycerol (OAG) is a versatile compound used in chemical synthesis for a variety of applications. As a synthetic intermediate, OAG plays a crucial role in the production of diverse chemical compounds, including pharmaceuticals, cosmetics, and specialty chemicals. Its unique chemical structure and reactivity make it a valuable building block for the creation of new molecules with specific properties and functionalities. In particular, OAG is commonly employed in the synthesis of lipid-based molecules, where its acetyl and oleoyl groups can be selectively modified to tailor the final product's properties. Additionally, OAG can serve as a substrate in enzymatic reactions for the production of bioactive compounds, making it an essential tool in the field of biocatalysis. In summary, 1-Oleoyl-2-acetyl-sn-glycerol is a versatile and valuable compound in chemical synthesis, offering a wide range of applications in the creation of novel molecules with tailored properties and functions.