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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)-

1,2-Cyclopentanedicarboxylic acid, cis-

OC(=O)[C@@H]1CCC[C@@H]1C(=O)O Request for Quotation
Chemical Name: 1,2-Cyclopentanedicarboxylic acid, cis-
CAS Number: 1461-96-7
Product Number: AG001DPL(AGN-PC-0O3955)
Synonyms:
MDL No:
Molecular Formula: C7H10O4
Molecular Weight: 158.1519

Identification/Properties

Properties
MP:
132-136℃
BP:
378.6 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
158.153g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
158.058g/mol
Monoisotopic Mass:
158.058g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
167
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


cis-Cyclopentane-1,2-dicarboxylic acid, also known as cis-CPDA, is a versatile compound commonly used in chemical synthesis. Its unique structure and properties make it a valuable building block in organic chemistry.In chemical synthesis, cis-CPDA is often employed as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its cyclic nature and carboxylic acid groups allow for facile derivatization through esterification, amidation, or other functionalization reactions.One of the notable applications of cis-CPDA is in the synthesis of cyclopentane-containing compounds, where it serves as a core component in the construction of complex molecular architectures. By strategically manipulating the functional groups on cis-CPDA, chemists can control the stereochemistry and regioselectivity of the final products.Additionally, cis-CPDA can be utilized in the preparation of chiral ligands for asymmetric catalysis, further expanding its utility in the field of organic synthesis. Its ability to participate in stereoselective reactions makes it a valuable tool for accessing enantiomerically pure compounds with high optical purity.Overall, cis-Cyclopentane-1,2-dicarboxylic acid plays a crucial role in modern chemical synthesis as a versatile and valuable building block for the efficient construction of diverse organic molecules.