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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)-

ethyl 3-aminocyclopentane-1-carboxylate

CCOC(=O)C1CCC(C1)N Request for Quotation
Chemical Name: ethyl 3-aminocyclopentane-1-carboxylate
CAS Number: 1187930-91-1
Product Number: AG0092GX(AGN-PC-0WO15J)
Synonyms:
MDL No: MFCD12913685
Molecular Formula: C8H15NO2
Molecular Weight: 157.2102

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Chemical Structure


Ethyl 3-aminocyclopentanecarboxylate is a versatile compound widely used in chemical synthesis as a building block for the preparation of various pharmaceutical and agrochemical products. Its unique structure and reactivity make it a valuable intermediate in organic synthesis processes, where it can undergo multiple functional group transformations to yield a diverse range of final products. In particular, Ethyl 3-aminocyclopentanecarboxylate is commonly employed in the synthesis of complex molecules with biological activity, making it an essential component in the development of new drugs and crop protection agents. Its ability to participate in diverse reactions, such as nucleophilic addition, acylation, and substitution, allows chemists to access a wide array of chemical modifications, enabling the creation of novel compounds with tailored properties and enhanced activities in various fields of research and industry.