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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[1.1.1]pentane-1-carboxylic acid, 3-phenyl-, methyl ester

COC(=O)C12CC(C1)(C2)c1ccccc1 Request for Quotation
Chemical Name: Bicyclo[1.1.1]pentane-1-carboxylic acid, 3-phenyl-, methyl ester
CAS Number: 83249-09-6
Product Number: AG00IDA7(AGN-PC-0OISSR)
Synonyms:
MDL No:
Molecular Formula: C13H14O2
Molecular Weight: 202.24906

Identification/Properties

Computed Properties
Molecular Weight:
202.253g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
202.099g/mol
Monoisotopic Mass:
202.099g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
269
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The unique structure of methyl 3-phenylbicyclo[1.1.1]pentane-1-carboxylate makes it a versatile compound in chemical synthesis. Its rigid and compact bicyclic framework offers opportunities for molecular manipulation and functionalization in organic reactions. This compound can serve as a building block for the synthesis of complex molecules and pharmaceuticals, where the bicyclic scaffold can impart specific structural and stereochemical properties. Additionally, the presence of the ester group allows for further derivatization through various chemical transformations, expanding its synthetic utility in the development of novel organic compounds.