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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)-

5-oxaspiro[2.4]heptane-1-carboxylic acid

OC(=O)C1CC21COCC2 Request for Quotation
Chemical Name: 5-oxaspiro[2.4]heptane-1-carboxylic acid
CAS Number: 1461705-13-4
Product Number: AG00HXH9(AGN-PC-0WOAOY)
Synonyms:
MDL No: MFCD18333861
Molecular Formula: C7H10O3
Molecular Weight: 142.1525

Identification/Properties

Computed Properties
Molecular Weight:
142.154g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
142.063g/mol
Monoisotopic Mass:
142.063g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
178
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 5-oxaspiro[2.4]heptane-1-carboxylic acid in chemical synthesis lies in its role as a versatile building block in organic chemistry. This compound serves as a key intermediate in the synthesis of various complex organic molecules, including pharmaceuticals, agrochemicals, and specialty chemicals.One of the primary uses of 5-oxaspiro[2.4]heptane-1-carboxylic acid is in the development of novel drugs and pharmaceuticals. By incorporating this compound into the molecular structure of drug candidates, chemists can modify the pharmacological properties, improve bioavailability, and enhance the overall efficacy of the final product. Additionally, the unique spirocyclic framework of this acid offers a valuable structural motif for creating diverse chemical entities with specific biological activities.Furthermore, in the field of agrochemicals, 5-oxaspiro[2.4]heptane-1-carboxylic acid can be utilized to synthesize insecticides, herbicides, and fungicides with improved performance and environmental safety profiles. Its involvement in the design of crop protection products highlights its importance in addressing global food security challenges and promoting sustainable agriculture practices.Overall, the strategic incorporation of 5-oxaspiro[2.4]heptane-1-carboxylic acid in chemical synthesis facilitates the development of innovative molecules with a wide range of applications, showcasing its significance in advancing research and innovation in the field of organic chemistry.