CAS 6011-14-9
:Acetonitrile, 2-amino-, hydrochloride (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
- See more synonyms
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 / itemFormula:C2H5ClN2Purity:98+%Color and Shape:White to pale brown, powderMolecular weight:92.532-Aminoacetonitrile hydrochloride
CAS:2-Aminoacetonitrile hydrochloridePurity:98%Molecular weight:92.53g/molAminoacetonitrile Hydrochloride
CAS:Formula:C2H4N2·HClPurity:>98.0%(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:92.53Aminoacetonitrile Hydrochloride
CAS:Controlled ProductApplications 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)Formula:C2H5ClN2Color and Shape:White To Off-WhiteMolecular weight:92.53Aminoacetonitrile hydrochloride
CAS:Formula:C2H5ClN2Purity:95%Color and Shape:Solid, Crystalline Powder or PowderMolecular weight: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.
Formula:C2H4N2·HClPurity:Min. 95%Color and Shape:White PowderMolecular weight:92.53 g/mol






