1. Home
  2. Propanoic acid, 2-hydroxy-, decylester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Propanoic acid, 2-hydroxy-, decylester

Request for Quotation
Chemical Name: Propanoic acid, 2-hydroxy-, decylester
CAS Number: 42175-34-8
Product Number: AG00D717(AGN-PC-0WAL5Q)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Propanoic acid, 2-hydroxy-, decylester is a versatile compound commonly utilized in chemical synthesis due to its unique properties and reactivity. This ester compound is frequently employed as a reagent in organic synthesis reactions to introduce the decyl group into various organic molecules. Its high purity and stability make it a preferred choice for researchers and chemists seeking controlled and efficient modification of molecules in the laboratory. In addition to its role as a chemical building block, propanoic acid, 2-hydroxy-, decylester can also serve as a precursor for the synthesis of complex organic compounds with applications in pharmaceuticals, fragrance development, and materials science. Its compatibility with a wide range of reaction conditions and its ability to participate in diverse chemical transformations highlight its importance in modern chemical synthesis strategies.