CAS 7682-20-4
:(S)-2-Aminobutiramida hidroclorídrica
Descrição:
(S)-2-Aminobutiramida hidroclorídrica é um composto de amina quiral caracterizado por seus grupos funcionais de amina e amida. É o sal hidroclorídrico de (S)-2-aminobutiramida, que é um bloco de construção importante na síntese orgânica e aplicações farmacêuticas. O composto geralmente aparece como um sólido cristalino branco a off-white, e é solúvel em água devido à presença do grupo hidrocloreto, que aumenta sua solubilidade. Sua estrutura molecular inclui uma espinha dorsal de quatro carbonos com um grupo amino (-NH2) e um grupo amida (-C(=O)NH2), contribuindo para sua reatividade e potencial para formar vários derivados. A quiralidade da molécula é significativa em sistemas biológicos, pois pode influenciar as propriedades farmacológicas e interações com alvos biológicos. (S)-2-Aminobutiramida hidroclorídrica é frequentemente usado em pesquisa e desenvolvimento, particularmente na síntese de peptídeos e outros compostos biologicamente ativos. O manuseio e as condições de armazenamento adequadas são essenciais para manter sua estabilidade e eficácia.
Fórmula:C4H11ClN2O
InChI:InChI=1/C4H10N2O.ClH/c1-2-3(5)4(6)7;/h3H,2,5H2,1H3,(H2,6,7);1H
Chave InChI:InChIKey=HDBMIDJFXOYCGK-DFWYDOINSA-N
SMILES:[C@@H](C(N)=O)(CC)N.Cl
Sinónimos:- (2S)-2-Aminobutanamide hydrochloride
- (2S)-2-aminobutanamide hydrochloride (1:1)
- (L)-2-Aminobutyramide hydrochloride
- (S)-2-Aminobutyramide HCL
- (S)-2-Aminobutyramide hydrochloride
- (S)-2-aminobutanamide hydrochloride
- 2-Aminobutanamide Hydrochloride (1:1)
- Abah
- Butanamide, 2-amino-, hydrochloride (1:1), (2S)-
- Butanamide, 2-amino-, monohydrochloride, (2S)-
- Butanamide, 2-amino-, monohydrochloride, (S)-
- Butyramide, 2-amino-, monohydrochloride, <span class="text-smallcaps">L</span>-
- H-Abu-NH2・HCl
- L-2-Amino Butanamide hydrochloride
- Levetiracetam's intermediate
- S(+)-2-amino butyramide HCl
- Butyramide, 2-amino-, monohydrochloride, L-
- Aminobutyramide Hydrochloride
- AMINOBUTYRIC ACID-NH2 HCL
- S(+)AminoButyramideHcl
- L-ALPHA-AMINOBUTYRIC ACID AMIDE HYDROCHLORIDE
- L-2-AMINO-BUTANOIC ACID HYDROCHLORIDE
- L-2-Amino
- Abu-Nh2 HCl
- (S)-2-sminobutanamide hydrochloride
- (S)-2-Aminobutanamide Monohydrochlorid
- l-2-aminobutanamide hydrochloride
- ALPHA-AMINOBUTYRIC ACID ALPHA-AMIDE HYDROCHLORIDE
- 2-AMINOBUTYRIC ACID AMIDE HYDROCHLORIDE
- (s)-2-amino-butylactamide
- H-ALPHA-ABU-NH2 HCL
- H-ABU(2)-NH2 HCL
- L-2-AMINOBUTANAMIDE HCL
- H-ABU(ALPHA)-NH2 HCL
- Ver mais sinónimos
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14 produtos.
(S)-2-Aminobutyramide Hydrochloride
CAS:Fórmula:C4H10N2O·HClPureza:>98.0%(HPLC)(N)Cor e Forma:White to Almost white powder to crystalPeso molecular:138.60Levetiracetam Related Compound B ((S)-2-aminobutanamide hydrochloride)
CAS:Acyclic amides (including acyclic carbamates) and their derivatives and salts thereof, nesoiFórmula:C4H10N2O·HClCor e Forma:White Cream PowderPeso molecular:102.07931Levetiracetam EP Impurity G HCl (Levetiracetam USP Related Compound B)
CAS:Fórmula:C4H10N2O·HClCor e Forma:White To Off-White SolidPeso molecular:102.14 36.46(S)-(+)-2-Aminobutanamide hydrochloride
CAS:(S)-(+)-2-Aminobutanamide hydrochloridePureza:98%Cor e Forma:SolidPeso molecular:138.60g/mol(S)-2-Aminobutyramide hydrochloride
CAS:Fórmula:C4H10N2OHClCor e Forma:White to off-white or tan crystalline powderPeso molecular:138.60(S)-2-Aminobutyramide Hydrochloride
CAS:Produto Controlado<p>Impurity Levetiracetam USP Related Compound B<br>Applications Levetiracetam USP Related Compound B<br></p>Fórmula:C4H10N2O·ClHCor e Forma:White To Off-WhitePeso molecular:138.60(S)-2-Aminobutyramide hydrochloride
CAS:Fórmula:C4H11ClN2OPureza:97%Cor e Forma:SolidPeso molecular:138.6(S)-2-Aminobutyramide hydrochloride
CAS:(S)-2-Aminobutyramide hydrochloride is a chiral amide compound, which is utilized primarily in scientific research settings. This compound is typically synthesized through the resolution of racemic mixtures or other specialized chemical processes that ensure the purity and stereospecificity required for research purposes.The mode of action of (S)-2-Aminobutyramide hydrochloride revolves around its role as an intermediate in chemical synthesis, serving as a building block for the production of more complex molecules. It has a noteworthy chiral configuration, which makes it an essential component in the formation of enantiomerically pure substances. This aspect is crucial in fields like pharmaceuticals, where stereochemistry can significantly impact biological activity.Its applications extend to various domains such as the synthesis of therapeutic agents, biochemical research, and the development of novel materials. Researchers value it for its ability to contribute to the fine-tuning of molecular assemblies, making it indispensable in studies focused on the interaction and function of chiral molecules. The hydrochloride form aids in its stability and solubility, which are important attributes for laboratory manipulation and experimentation.Fórmula:C4H10N2O•HClPureza:Min. 95%Cor e Forma:White PowderPeso molecular:138.6 g/molH-Abu-NH2 HCl
CAS:<p>H-Abu-NH2 HCl is a useful organic compound for research related to life sciences. The catalog number is T66187 and the CAS number is 7682-20-4.</p>Fórmula:C4H11ClN2OCor e Forma:SolidPeso molecular:138.6














