CAS 6011-14-9
:Acetonitrila, 2-amino-, cloridrato (1:1)
- 2-Aminoacetonitrile hydrochloride
- 2-AminoacetonitrileHydrochloride
- Acetonitrile, 2-amino-, hydrochloride (1:1)
- Acetonitrile, amino-, monohydrochloride
- Alpha-Aminoacetonitrilehydrochloride
- Amino acetonitrile HCL
- Amino-Acetonitrile sulfate
- Amino-Acetonitrilmonohydrochloride
- Aminoacetonitrile hydrochloride
- Aminoacetonitrile monohydrochloride
- Aminoacetonitrilemonohydrochloride
- Cyanomethanamine hydrochloride
- Cyanomethanaminium Chloride
- Glycinonitrile,Monohydrochloride
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Aminoacetonitrile hydrochloride, 98+%
CAS:Used as pharmaceutical intermediates, organic synthetic raw material transportation. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / itemFórmula:C2H5ClN2Pureza:98+%Cor e Forma:White to pale brown, powderPeso molecular:92.532-Aminoacetonitrile hydrochloride
CAS:2-Aminoacetonitrile hydrochloridePureza:98%Peso molecular:92.53g/molAminoacetonitrile Hydrochloride
CAS:Fórmula:C2H4N2·HClPureza:>98.0%(T)Cor e Forma:White to Light yellow powder to crystalPeso molecular:92.53Aminoacetonitrile Hydrochloride
CAS:Produto ControladoApplications Aminoacetonitrile is a useful synthetic intermediate. It is a reagent used to synthesize dipeptide nitriles as reversible and potent cathepsin S inhibitors. It can also used to prepare substituted cyclic ureas as possible HIV protease inhibitors.
References Ward, Y., et al.: J. Med. Chem., 45, 5471 (2002); Wilkerson, W., et al.: J. Med. Chem., 40, 4079 (1997)Fórmula:C2H5ClN2Cor e Forma:White To Off-WhitePeso molecular:92.53Aminoacetonitrile hydrochloride
CAS:Fórmula:C2H5ClN2Pureza:95%Cor e Forma:Solid, Crystalline Powder or PowderPeso molecular:92.53Aminoacetonitrile HCl
CAS:Aminoacetonitrile HCl is a chemical compound that has been used in pharmaceutical preparations for the treatment of autoimmune diseases. It has been shown to inhibit the growth of Streptococcus faecalis and other bacteria by forming reversible covalent bonds with proteins, which inhibits enzymatic activity and protein synthesis. Aminoacetonitrile HCl also reacts with amino groups on proteins, leading to an acylation reaction that prevents interactions with other molecules. This effect is specific to toll-like receptor (TLR) signaling, which plays a role in the immune response to infection. Aminoacetonitrile HCl has also been shown to be effective against cancer cells and restenosis in animal models.
Fórmula:C2H4N2·HClPureza:Min. 95%Cor e Forma:White PowderPeso molecular:92.53 g/mol






