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CAS 96886-56-5

:

(2R)-2-Amino-2-methyl-4-pentenoic acid

Description:
(2R)-2-Amino-2-methyl-4-pentenoic acid, also known as a derivative of amino acids, is characterized by its unique structure that includes an amino group, a carboxylic acid group, and a branched aliphatic chain. This compound features a double bond in its pentenoic acid moiety, which contributes to its reactivity and potential biological activity. The presence of the amino group makes it a basic compound, while the carboxylic acid group imparts acidic properties. Its chirality, indicated by the (2R) designation, suggests that it exists as one of two enantiomers, which can exhibit different biological activities. This compound may be involved in various biochemical pathways and could serve as a building block for more complex molecules in synthetic organic chemistry. Its CAS number, 96886-56-5, allows for precise identification in chemical databases. Overall, (2R)-2-Amino-2-methyl-4-pentenoic acid is of interest in both research and potential applications in pharmaceuticals and biochemistry.
Formula:C6H11NO2
InChI:InChI=1/C6H11NO2/c1-3-4-6(2,7)5(8)9/h3H,1,4,7H2,2H3,(H,8,9)/t6-/m1/s1
InChI key:InChIKey=QMBTZYHBJFPEJB-ZCFIWIBFSA-N
SMILES:[C@@](CC=C)(C(O)=O)(C)N
Synonyms:
  • (2R)-2-Amino-2-methyl-4-pentenoic acid
  • (2R)-2-Azaniumyl-2-methylpent-4-enoate
  • (2R)-2-amino-2-methylpent-4-enoic acid
  • (R)-(+)-α-Allylalanine
  • 4-Pentenoic acid, 2-amino-2-methyl-, (2R)-
  • 4-Pentenoic acid, 2-amino-2-methyl-, (R)-
  • D-alpha-Allylalanine
  • H-alpha-All-L-Ala-OH
  • (R)-2-(2'-propylenyl)alanine, >97%
  • (S)-2-Amino-2-methyl-4-pentenoic acid
  • See more synonyms
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