Hexadecanoic acid, 3-chloro-2-hydroxypropyl ester


Chemical Name: Hexadecanoic acid, 3-chloro-2-hydroxypropyl ester
CAS Number: 30557-04-1
Product Number: AG0030JN(AGN-PC-07Y4U0)
Synonyms:
MDL No:
Molecular Formula: C19H37ClO3
Molecular Weight: 348.9483

Identification/Properties


Properties
MP:
27-28°C
Storage:
-10 ℃;
Form:
Liquid
Computed Properties
Molecular Weight:
348.952g/mol
XLogP3:
7.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
18
Exact Mass:
348.243g/mol
Monoisotopic Mass:
348.243g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
259
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

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Chemical Structure



1-Chloro-3,3-dihydroxynonadecan-4-one, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a crucial building block in the development of various organic molecules and materials due to its chloro and hydroxy functional groups.In chemical synthesis, 1-Chloro-3,3-dihydroxynonadecan-4-one can be utilized as a key intermediate for the creation of complex organic compounds. The chloro group provides a site for nucleophilic substitution reactions, allowing for the introduction of different functional groups or the modification of the compound's structure. The two hydroxy groups also offer opportunities for further derivatization, such as esterification or ether formation, leading to the synthesis of diverse chemical entities.Moreover, the long carbon chain present in 1-Chloro-3,3-dihydroxynonadecan-4-one imparts lipophilic properties to the compound, making it suitable for applications in material science, such as in the production of surfactants, emulsifiers, and lipid-based formulations. Additionally, the presence of the carbonyl group in the molecule enables it to participate in condensation reactions for the formation of ketones or aldehydes, further expanding its synthetic utility.Overall, 1-Chloro-3,3-dihydroxynonadecan-4-one plays a crucial role in chemical synthesis by offering a diverse range of functional groups and structural elements that can be harnessed to create novel organic compounds and materials with tailored properties and applications.