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(R)-ALPHA-METHYLVALINAMIDE

  • Name(R)-ALPHA-METHYLVALINAMIDE
  • CAS90376-98-0
  • Purity99%
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1.What is the (R)-ALPHA-METHYLVALINAMIDE ?

(R)-ALPHA-METHYLVALINAMIDE is an organic compound that belongs to the class of amides, characterized by the replacement of the carboxyl group, COOH, with a carboxamide group, CONR2. The "R" in its name signifies the configuration of the chiral center, which is an important aspect of its orientation. The term "Alpha-Methylvalinamide" refers to the specific structural components of the compound, including the Alpha-Methylvaline molecule and the amide functional group attached to it. This chemical is valuable for its use in various biological studies and chemical reactions.

2.What is the CAS number for (R)-ALPHA-METHYLVALINAMIDE ?

The CAS number of (R)-ALPHA-METHYLVALINAMIDE is 90376-98-0.

3.What are another words for (R)-ALPHA-METHYLVALINAMIDE ?

Synonyms?for?(R)-ALPHA-METHYLVALINAMIDE 90376-98-0:Butanamide,2-amino-2,3-dimethyl-, (R)-; (+)-2-Amino-2,3-dimethylbutyramide;(R)-2-Amino-2,3-dimethylbutanamide

4.What is (R)-ALPHA-METHYLVALINAMIDE (90376-98-0) used for?

Used in Pharmaceutical Industry:
(R)-ALPHA-METHYLVALINAMIDE is used as an intermediate in the synthesis of pharmaceutical compounds for its unique structural properties and reactivity, contributing to the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
(R)-ALPHA-METHYLVALINAMIDE is utilized as a research chemical in various chemical studies, allowing scientists to explore its properties, reactivity, and potential applications in the synthesis of other organic compounds.
Used in Biochemical Applications:
(R)-ALPHA-METHYLVALINAMIDE is employed in biochemical research to investigate its interactions with biological systems, potentially leading to insights into its role in biological processes and the development of bioactive molecules.

Relevant articles related to (R)-ALPHA-METHYLVALINAMIDE:

Article

Source

Synthesis of dipeptides containing α-substituted amino acids; their use as chiral ligands in Lewis-acid-catalyzed reactions

Kaptein, Bernard,Monaco, Vania,Broxterman, Quirinus B.,Schoemaker, Hans E.,Kamphuis, Johan

, p. 231 - 238 (2007/10/02)

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