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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)-

Bicyclo[2.2.1]heptane-1,4-dicarboxylic acid, monomethyl ester

COC(=O)C12CCC(C2)(CC1)C(=O)O Request for Quotation
Chemical Name: Bicyclo[2.2.1]heptane-1,4-dicarboxylic acid, monomethyl ester
CAS Number: 15448-77-8
Product Number: AG00389K(AGN-PC-0JD0LR)
Synonyms:
MDL No:
Molecular Formula: C10H14O4
Molecular Weight: 198.2158

Identification/Properties

Computed Properties
Molecular Weight:
198.218g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
198.089g/mol
Monoisotopic Mass:
198.089g/mol
Topological Polar Surface Area:
63.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
287
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound Bicyclo[2.2.1]heptane-1,4-dicarboxylic acid, monomethyl ester is commonly utilized in chemical synthesis processes as a versatile building block. Its unique molecular structure, characterized by a bicyclic core and carboxylic acid functionality, imparts distinct reactivity profiles that make it valuable in the formation of various organic compounds.In chemical synthesis, Bicyclo[2.2.1]heptane-1,4-dicarboxylic acid, monomethyl ester serves as a key intermediate for the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and materials. Its cycloalkane framework provides rigidity and stereochemical control, which are crucial for directing the regioselectivity and stereochemistry of subsequent reactions.Furthermore, the presence of carboxylic acid groups in this compound allows for facile derivatization through esterification, amidation, or other chemical transformations. These functional groups enable the attachment of various substituents, facilitating the modification of physical and chemical properties of the final products.Overall, the strategic incorporation of Bicyclo[2.2.1]heptane-1,4-dicarboxylic acid, monomethyl ester in chemical synthesis offers synthetic chemists a powerful tool for the construction of diverse molecular architectures with precise control over stereochemistry and functional group distribution.