CAS 7682-20-4
:(S)-2-Aminobutiramida hidrocloruro
Descripción:
(S)-2-Aminobutiramida hidrocloruro es un compuesto de amina quiral caracterizado por sus grupos funcionales de amina y amida. Es la sal hidroclorídica de (S)-2-aminobutiramida, que es un bloque de construcción importante en la síntesis orgánica y aplicaciones farmacéuticas. El compuesto típicamente aparece como un sólido cristalino blanco a blanco sucio, y es soluble en agua debido a la presencia del grupo hidrocloruro, que mejora su solubilidad. Su estructura molecular incluye un esqueleto de cuatro carbonos con un grupo amino (-NH2) y un grupo amida (-C(=O)NH2), lo que contribuye a su reactividad y potencial para formar varios derivados. La quiralidad de la molécula es significativa en sistemas biológicos, ya que puede influir en las propiedades farmacológicas e interacciones con objetivos biológicos. (S)-2-Aminobutiramida hidrocloruro se utiliza a menudo en investigación y desarrollo, particularmente en la síntesis de péptidos y otros compuestos biológicamente activos. Las condiciones adecuadas de manejo y almacenamiento son esenciales para mantener su estabilidad y eficacia.
Fórmula:C4H11ClN2O
InChI:InChI=1/C4H10N2O.ClH/c1-2-3(5)4(6)7;/h3H,2,5H2,1H3,(H2,6,7);1H
Clave 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 más sinónimos
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Encontrado 14 productos.
(S)-2-Aminobutyramide Hydrochloride
CAS:Fórmula:C4H10N2O·HClPureza:>98.0%(HPLC)(N)Forma y color: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·HClForma y color:White Cream PowderPeso molecular:102.07931Levetiracetam EP Impurity G HCl (Levetiracetam USP Related Compound B)
CAS:Fórmula:C4H10N2O·HClForma y color:White To Off-White SolidPeso molecular:102.14 36.46(S)-(+)-2-Aminobutanamide hydrochloride
CAS:(S)-(+)-2-Aminobutanamide hydrochloridePureza:98%Forma y color:SolidPeso molecular:138.60g/mol(S)-2-Aminobutyramide hydrochloride
CAS:Fórmula:C4H10N2OHClForma y color:White to off-white or tan crystalline powderPeso molecular:138.60(S)-2-Aminobutyramide Hydrochloride
CAS:Producto controlado<p>Impurity Levetiracetam USP Related Compound B<br>Applications Levetiracetam USP Related Compound B<br></p>Fórmula:C4H10N2O·ClHForma y color:White To Off-WhitePeso molecular:138.60(S)-2-Aminobutyramide hydrochloride
CAS:Fórmula:C4H11ClN2OPureza:97%Forma y color: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%Forma y color: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:C4H11ClN2OForma y color:SolidPeso molecular:138.6














