
CAS 1229025-32-4
:Carbamic acid, N-[(1S)-2-amino-1-methylethyl]-, methyl ester, hydrochloride (1:1)
Description:
Carbamic acid, N-[(1S)-2-amino-1-methylethyl]-, methyl ester, hydrochloride (1:1) is a chemical compound characterized by its structure, which includes a carbamic acid moiety linked to a methyl ester and an amino group. This compound typically appears as a white to off-white solid and is soluble in water due to the presence of the hydrochloride salt form, which enhances its solubility and stability. The presence of the amino group suggests potential basic properties, while the carbamic acid structure indicates it may exhibit both acidic and basic characteristics. This compound may be of interest in pharmaceutical applications, particularly in the development of drugs that target specific biological pathways. Its specific stereochemistry, indicated by the (1S) designation, may influence its biological activity and interactions. As with many chemical substances, safety data sheets should be consulted for handling and toxicity information, as well as any regulatory considerations associated with its use.
Formula:C5H12N2O2·ClH
InChI:InChI=1S/C5H12N2O2.ClH/c1-4(3-6)7-5(8)9-2;/h4H,3,6H2,1-2H3,(H,7,8);1H/t4-;/m0./s1
InChI key:InChIKey=DTVBZYSSZUCODC-WCCKRBBISA-N
SMILES:N([C@H](CN)C)C(OC)=O.Cl
Synonyms:- Carbamic acid, N-[(1S)-2-amino-1-methylethyl]-, methyl ester, hydrochloride (1:1)
- (S)-Methyl (1-aminopropan-2-yl)carbamate hydrochloride
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Found 4 products.
Carbamic acid, N-[(1S)-2-amino-1-methylethyl]-, methyl ester, hydrochloride (1:1)
CAS:Formula:C5H13ClN2O2Purity:97%Color and Shape:SolidMolecular weight:168.6219methyl (S)-(1-Aminopropan-2-yl)carbamate hydrochloride
CAS:methyl (S)-(1-Aminopropan-2-yl)carbamate hydrochloridePurity:97%Molecular weight:168.62g/mol(S)-Methyl (1-aminopropan-2-yl)carbamate hydrochloride
CAS:<p>(S)-Methyl (1-aminopropan-2-yl)carbamate hydrochloride is a structural formula of a chemical which is chemically an organic compound in laboratories. Encorafenib is an inhibitor of the protein kinase B (AKT). This inhibition reduces the phosphorylation of downstream proteins, such as glycogen synthase kinase 3β, thereby inhibiting the growth and survival of tumor cells.</p>Formula:C5H13ClN2O2Purity:Min. 95%Molecular weight:168.62 g/mol



