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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)-

L-Ascorbic acid, 6-octadecanoate

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Chemical Name: L-Ascorbic acid, 6-octadecanoate
CAS Number: 10605-09-1
Product Number: AG003R7X(AGN-PC-0OVIAN)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
117 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
442.593g/mol
XLogP3:
7.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
20
Exact Mass:
442.293g/mol
Monoisotopic Mass:
442.293g/mol
Topological Polar Surface Area:
113A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
544
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


L-Ascorbic acid 6-stearate is a specialized form of Vitamin C that finds significant application in chemical synthesis processes. Due to its unique structure and properties, this compound serves as a multifunctional reagent in various reactions and transformations. In chemical synthesis, L-ascorbic acid 6-stearate functions as a versatile agent for promoting various organic reactions, particularly in the formation of esters, amides, and other derivatives through esterification or amidation reactions. Its ability to act as both a reducing agent and a catalyst makes it a valuable tool in the synthesis of a wide range of compounds. Furthermore, the lipophilic nature of the stearate group allows for enhanced solubility in organic solvents, facilitating its incorporation into non-aqueous reaction systems. This characteristic enables L-ascorbic acid 6-stearate to participate in reactions that require a non-polar environment, thereby expanding its utility in different chemical transformations. Overall, the application of L-ascorbic acid 6-stearate in chemical synthesis offers researchers a versatile and effective tool to facilitate the efficient formation of diverse organic compounds.