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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)-

Pentanoic acid, 2-furanylmethyl ester

CCCCC(=O)OCc1ccco1 Request for Quotation
Chemical Name: Pentanoic acid, 2-furanylmethyl ester
CAS Number: 36701-01-6
Product Number: AG00BY50(AGN-PC-0JL4RL)
Synonyms:
MDL No:
Molecular Formula: C10H14O3
Molecular Weight: 182.2164

Identification/Properties

Properties
BP:
230.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H227-H302
Precautionary Statements:
P210-P280-P370+P378-P403+P235-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Furan-2-ylmethyl pentanoate is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its structure, consisting of a furan ring attached to a pentanoate group, enables it to participate in a range of synthetic transformations and functional group manipulations.One of the key applications of Furan-2-ylmethyl pentanoate is in the synthesis of heterocyclic compounds. The furan ring provides a reactive site for cyclization reactions, leading to the formation of complex structures with diverse biological activities. This compound can also act as a carbonyl equivalent in various synthetic strategies, allowing for the introduction of functional groups or stereochemical elements into the final products.Furthermore, Furan-2-ylmethyl pentanoate can be employed as a protecting group in organic synthesis to safeguard specific functional groups during chemical transformations. By selectively deprotecting the compound under specific conditions, chemists can control the order of reactions and ensure the desired regioselectivity or stereoselectivity in complex molecule assembly.Overall, the versatility and reactivity of Furan-2-ylmethyl pentanoate make it a crucial tool in the toolkit of synthetic chemists, enabling the efficient construction of intricate molecular architectures and the development of novel chemical entities with potential applications in various fields.