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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)-

2-Heptanol, benzoate

OC(=O)c1ccccc1.CCCCCC(O)C Request for Quotation
Chemical Name: 2-Heptanol, benzoate
CAS Number: 6624-59-5
Product Number: AG00FR7W(AGN-PC-0BSATN)
Synonyms:
MDL No:
Molecular Formula: C14H22O3
Molecular Weight: 238.32268

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Chemical Structure


2-Heptanol, 2-benzoate is a versatile compound commonly utilized in chemical synthesis processes. This compound serves as a crucial intermediate in the production of various organic compounds due to its unique structure and properties. Its application in chemical synthesis is notable for its role as a precursor in the creation of fragrances, pharmaceuticals, and other fine chemicals. The presence of the benzoate group in 2-Heptanol further enhances its reactivity and compatibility in different chemical reactions, making it a valuable component in diverse synthesis pathways. Its ability to undergo esterification reactions further expands its utility in the formation of esters, which are essential in the development of numerous products across industries. In essence, the incorporation of 2-Heptanol, 2-benzoate in chemical synthesis processes underscores its significance as a pivotal building block for the creation of complex molecular structures with diverse applications.