CAS 7324-11-0
:(2S)-2-Aminobutanamide
Description:
(2S)-2-Aminobutanamide, with the CAS number 7324-11-0, is an organic compound characterized by its amine and amide functional groups. It is a chiral molecule, meaning it has a specific stereochemistry, denoted by the (2S) configuration, which indicates the spatial arrangement of its atoms. This compound is typically a white to off-white solid at room temperature and is soluble in polar solvents due to the presence of the amine and amide groups, which can engage in hydrogen bonding. (2S)-2-Aminobutanamide is often used in biochemical research and pharmaceutical applications, particularly in the synthesis of various bioactive molecules. Its structure allows it to participate in various chemical reactions, including peptide bond formation, making it relevant in the study of amino acids and proteins. Additionally, the compound's properties may vary based on its purity and the presence of other functional groups in a given reaction context. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C4H10N2O
InChI:InChI=1S/C4H10N2O/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H2,6,7)/t3-/m0/s1
InChI key:InChIKey=HNNJFUDLLWOVKZ-VKHMYHEASA-N
SMILES:[C@@H](C(N)=O)(CC)N
Synonyms:- (2S)-2-Aminobutanamide
- (2S)-2-Aminobutyramide
- (S)-2-Aminobutanamide
- (S)-2-Aminobutyramide
- <span class="text-smallcaps">L</span>-2-Amino-n-butanamide
- <span class="text-smallcaps">L</span>-Butyrinamide
- <span class="text-smallcaps">L</span>-α-aminobutyramide
- Butanamide, 2-amino-, (2S)-
- Butanamide, 2-amino-, (S)-
- Butyramide, 2-amino-, <span class="text-smallcaps">L</span>-
- L-2-Amino-n-butanamide
- See more synonyms
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Found 5 products.
H-Abu-NH₂
CAS:<p>Bachem ID: 4029269.</p>Formula:C4H10N2OPurity:> 99%Color and Shape:White PowderMolecular weight:102.14L-2-Aminobutanamide
CAS:<p>L-2-Aminobutanamide is a compound that is used as an industrial preparation and as a reagent in kinetic studies. It has been shown to be effective in the analytical method for the determination of hydrochloric acid in titration, with a detection limit of 0.1%. L-2-Aminobutanamide can also be used to produce asymmetric synthesis by adding it with sodium hydroxide solution or hydroxide solution and using chromatographic science. This compound has been shown to have antibacterial effects on Brucella, which can be attributed to its ability to inhibit protein synthesis and disrupt cell membrane integrity. L-2-Aminobutanamide is a chiral compound that can exist in two different forms, L -(+)-2-aminobutanamide or D -(-)-2-aminobutanamide.</p>Formula:C4H10N2OPurity:Min. 95%Molecular weight:102.14 g/mol




