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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)-

4-Cyclopentene-1,3-diol, monoacetate, (1R,3S)-

O[C@@H]1C=C[C@@H](C1)O.CC(=O)O Request for Quotation
Chemical Name: 4-Cyclopentene-1,3-diol, monoacetate, (1R,3S)-
CAS Number: 60176-77-4
Product Number: AG00E9SD(AGN-PC-0OD24L)
Synonyms:
MDL No:
Molecular Formula: C7H12O4
Molecular Weight: 160.16778

Identification/Properties

Computed Properties
Molecular Weight:
142.154g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
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:
162
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


(1S,4R)-Cis-4-acetoxy-2-cyclopenten-1-ol, commonly known as $name$, is a versatile compound that plays a crucial role in chemical synthesis. This compound is widely utilized as a chiral building block in organic reactions due to its unique stereochemistry and functional groups.In chemical synthesis, (1S,4R)-Cis-4-acetoxy-2-cyclopenten-1-ol serves as an important intermediate in the preparation of various pharmaceuticals, agrochemicals, and natural products. Its specific stereochemical configuration allows for the creation of complex molecules with high stereochemical purity, making it highly valuable in the field of asymmetric synthesis.Furthermore, the presence of an acetoxy group in the compound provides opportunities for further derivatization through various chemical transformations. This enables chemists to modify the structure of the compound to introduce desired functionalities or create novel molecules with specific properties.Overall, (1S,4R)-Cis-4-acetoxy-2-cyclopenten-1-ol is a key component in the toolbox of synthetic chemists, offering a wide range of applications in the efficient and selective synthesis of structurally diverse compounds.