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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, 2-chloroethyl ester

CCCCCCCCCCCCCCCCCC(=O)OCCCl Request for Quotation
Chemical Name: Octadecanoic acid, 2-chloroethyl ester
CAS Number: 1119-75-1
Product Number: AG00388M(AGN-PC-0JL9VJ)
Synonyms:
MDL No:
Molecular Formula: C20H39ClO2
Molecular Weight: 346.9755

Identification/Properties

Computed Properties
Molecular Weight:
346.98g/mol
XLogP3:
9.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
19
Exact Mass:
346.264g/mol
Monoisotopic Mass:
346.264g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
244
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloroethyl stearate, also known as chloroethyl octadecanoate, is a chemical compound commonly utilized in chemical synthesis processes. This versatile compound is often employed as a reactive intermediate in the production of various organic compounds. Its unique structure, combining a chloroethyl group with a stearate moiety, allows it to participate in a wide range of chemical reactions, making it a valuable building block in organic synthesis.In chemical synthesis, 2-Chloroethyl stearate is frequently employed for its ability to introduce the chloroethyl functional group into target molecules. This group can serve as a versatile handle for further derivatization, enabling the creation of more complex organic structures. Additionally, the stearate moiety can impart unique physicochemical properties to the resulting compounds, making them suitable for specific applications.One common application of 2-Chloroethyl stearate is in the synthesis of surfactants and emulsifiers. By incorporating this compound into the structure of surfactants, manufacturers can tailor the properties of these compounds to achieve desired surface-active characteristics. Furthermore, the presence of the stearate group can enhance the stability and performance of the final surfactant products.Moreover, 2-Chloroethyl stearate is utilized in the production of specialty chemicals such as pharmaceutical intermediates, agrochemicals, and polymer additives. Its reactivity and compatibility with a wide range of functional groups make it a valuable tool for chemists seeking to create novel compounds with specific properties.Overall, 2-Chloroethyl stearate plays a crucial role in chemical synthesis by serving as a key building block for the creation of diverse organic compounds with tailored properties and functions. Its versatility and reactivity make it a valuable asset in the toolkit of synthetic chemists working across various industries.