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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)-

14-Pentadecenoic acid

C=CCCCCCCCCCCCCC(=O)O Request for Quotation
Chemical Name: 14-Pentadecenoic acid
CAS Number: 17351-34-7
Product Number: AG001YZD(AGN-PC-0JSMTT)
Synonyms:
MDL No:
Molecular Formula: C15H28O2
Molecular Weight: 240.3816

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
240.387g/mol
XLogP3:
6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
13
Exact Mass:
240.209g/mol
Monoisotopic Mass:
240.209g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
187
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Pentadec-14-enoic acid, also known as palmitoleic acid, plays a crucial role in chemical synthesis as a versatile building block in organic reactions. Due to its unique structure containing a double bond at the 14th carbon atom, this fatty acid is highly valuable in the production of various compounds. In chemical synthesis, Pentadec-14-enoic acid serves as a precursor for the synthesis of esters, amides, and other complex molecules through processes such as esterification, amidation, and hydrogenation. Additionally, its double bond can undergo functionalization reactions, enabling the introduction of different functional groups for tailored chemical structures. This makes Pentadec-14-enoic acid a valuable ingredient in the creation of pharmaceuticals, cosmetics, and specialty chemicals, where precise control over molecular structure and properties is essential.