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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)-

(1S,2S)-2-([(TERT-BUTOXY)CARBONYL]AMINO)CYCLOBUTANE-1-CARBOXYLIC ACI

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Chemical Name: (1S,2S)-2-([(TERT-BUTOXY)CARBONYL]AMINO)CYCLOBUTANE-1-CARBOXYLIC ACI
CAS Number: 951173-39-0
Product Number: AG01DY34(AGN-PC-0WAKGS)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


The (1S,2S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclobutanecarboxylic acid, also referred to as $name$, plays an essential role in chemical synthesis as a chiral building block. This compound is widely utilized in asymmetric synthesis to introduce stereochemical control into the formation of chemical structures. By incorporating this chiral compound into reactions, chemists can access enantiomerically pure products, crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure contributes to the formation of complex molecules with high regio- and stereo-selectivity, making it a valuable tool in organic synthesis strategies.