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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)-

(R)-N-Boc-2-(3'-butenyl)glycine

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Chemical Name: (R)-N-Boc-2-(3'-butenyl)glycine
CAS Number: 219819-76-8
Product Number: AG00BG8Z(AGN-00BG3F)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


(2R)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-5-hexenoic acid is a valuable compound in chemical synthesis due to its versatile applications. This compound is commonly utilized as a chiral building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure, containing both a carboxylic acid and an amino group, allows for selective functionalization and incorporation into complex molecular scaffolds. Furthermore, the (2R) stereochemistry of this compound confers specific reactivity and selectivity in reactions, enabling precise control over the stereochemistry of the final products. In organic synthesis, (2R)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-5-hexenoic acid serves as a versatile intermediate for the construction of biologically active molecules and provides synthetic chemists with a powerful tool for creating structurally diverse compounds with defined stereochemistry.