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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)-

Octadecanoic acid, oxiranylmethyl ester

CCCCCCCCCCCCCCCCCC(=O)OCC1OC1 Request for Quotation
Chemical Name: Octadecanoic acid, oxiranylmethyl ester
CAS Number: 7460-84-6
Product Number: AG003QSB(AGN-PC-0JL547)
Synonyms:
MDL No:
Molecular Formula: C21H40O3
Molecular Weight: 340.5405

Identification/Properties

Properties
MP:
53 °C
BP:
424.7°C at 760 mmHg
Storage:
-10 ℃;
Form:
Solid
Refractive Index:
1.5192 (estimate)
Computed Properties
Molecular Weight:
340.548g/mol
XLogP3:
8.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
19
Exact Mass:
340.298g/mol
Monoisotopic Mass:
340.298g/mol
Topological Polar Surface Area:
38.8A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
291
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


Oxiran-2-ylmethyl stearate is a versatile compound that finds its application in various chemical synthesis processes. Due to the presence of the oxirane ring, this compound serves as an important building block in the creation of various organic molecules. It can act as a precursor for the synthesis of other compounds by undergoing ring-opening reactions with nucleophiles. Additionally, Oxiran-2-ylmethyl stearate can be utilized in the production of polymers and surfactants, where its unique structure can impart specific properties to the final products. In pharmaceutical synthesis, this compound can be employed for the preparation of drug molecules or as an intermediate in the synthesis of active pharmaceutical ingredients. Overall, Oxiran-2-ylmethyl stearate plays a crucial role in enabling the creation of diverse compounds in the field of chemical synthesis.