1-(2-Amino-3-methylbut-1-yl)-1H-imidazole dihydrochloride

Base Information

• Chemical Name: 1-(2-Amino-3-methylbut-1-yl)-1H-imidazole dihydrochloride
• CAS No.: 1172472-37-5
• Molecular Formula: C₈H₁₅N₃*ClH
• Molecular Weight: 189.688
• Hs Code.: 2921199990
• DSSTox Substance ID: DTXSID10592103
• Mol file: 1172472-37-5.mol

Synonyms:1172472-37-5;1-(2-Amino-3-methylbut-1-yl)-1H-imidazole dihydrochloride;1-(1H-Imidazol-1-yl)-3-methylbutan-2-amine dihydrochloride;2-IMIDAZOL-1-YL-1-ISOPROPYL-ETHYLAMINE 2HCL;1-imidazol-1-yl-3-methylbutan-2-amine;dihydrochloride;1-(1H-Imidazol-1-yl)-3-methylbutan-2-aminedihydrochloride;2-IMIDAZOL-1-YL-1-ISOPROPYL-ETHYLAMINE DIHYDROCHLORIDE;2-Imidazol-1-yl-1-isopropyl-ethylamine DiHCl;DTXSID10592103;AR1136;MFCD04117727;AKOS027253708;AS-45036;CS-0171933;A908569;2-(1H-Imidazol-1-yl)-1-isopropylethylamine dihydrochloride;1-(1H-Imidazol-1-yl)-3-methylbutan-2-amine--hydrogen chloride (1/2)

Chemical Property of 1-(2-Amino-3-methylbut-1-yl)-1H-imidazole dihydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 225.0799529
• Heavy Atom Count: 13
• Complexity: 114

Purity/Quality:

99% ^*data from raw suppliers

2-Imidazol-1-yl-1-isopropyl-ethylamineDihydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C)C(CN1C=CN=C1)N.Cl.Cl

Technology Process of 1-(2-Amino-3-methylbut-1-yl)-1H-imidazole dihydrochloride

There total 1 articles about 1-(2-Amino-3-methylbut-1-yl)-1H-imidazole dihydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C13H23N3O2 → C8H15N3*ClH (1172472-37-5)

Guidance literature:

With hydrogenchloride; In ethanol; at 20 ℃;

DOI:10.1016/j.ejmech.2019.05.047

Refernces