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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)-

1,3-Cyclopentanedicarboxylic acid, monomethyl ester, (1R-cis)-

COC(=O)[C@@H]1CC[C@@H](C1)C(=O)[O-] Request for Quotation
Chemical Name: 1,3-Cyclopentanedicarboxylic acid, monomethyl ester, (1R-cis)-
CAS Number: 96443-42-4
Product Number: AG00IJT8(AGN-PC-0OODM7)
Synonyms:
MDL No:
Molecular Formula: C8H11O4-
Molecular Weight: 171.17054

Identification/Properties

Computed Properties
Molecular Weight:
172.18g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
172.074g/mol
Monoisotopic Mass:
172.074g/mol
Topological Polar Surface Area:
63.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
199
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (1S,3R)-3-(Methoxycarbonyl)cyclopentanecarboxylic acid is a versatile compound commonly used in chemical synthesis for its unique stereochemical properties and functional group reactivity. In organic chemistry, this compound serves as a valuable building block for the synthesis of complex molecules due to its ability to undergo various reactions and transformations.One of the key applications of (1S,3R)-3-(Methoxycarbonyl)cyclopentanecarboxylic acid is in the synthesis of pharmaceutical intermediates and natural products. Its specific stereochemistry and functional groups make it an ideal starting material for the preparation of chiral compounds with potential biological activity. By utilizing this compound in synthesis, chemists can access structurally diverse molecules that may have therapeutic or diagnostic applications.Additionally, (1S,3R)-3-(Methoxycarbonyl)cyclopentanecarboxylic acid can be used in the development of new materials, such as polymers or catalysts, where its structural features can impart specific properties or functions. Its reactivity towards various chemical reactions allows for the introduction of desired modifications or functional groups, enabling the tailoring of the final product for specific applications.Overall, the (1S,3R)-3-(Methoxycarbonyl)cyclopentanecarboxylic acid plays a crucial role in chemical synthesis by offering a platform for the construction of complex molecules and the creation of novel materials with tailored properties. Its versatility and reactivity make it a valuable tool for researchers and chemists seeking to explore new avenues in organic chemistry and drug discovery.