Description

4-(((1,1-Dimethylethoxy)carbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid (CAS: 128293-64-1) is a high-purity, synthetic imidazole derivative designed for advanced research and pharmaceutical applications. This compound, with the molecular formula C₁₀H₁₅N₃O₄, features a tert-butoxycarbonyl (Boc) protected amino group and a carboxylic acid functionality, making it a versatile intermediate in organic synthesis and medicinal chemistry. Its IUPAC name is 1-methyl-4-[(2-methylpropan-2-yl)oxycarbonylamino]imidazole-2-carboxylic acid. Ideal for peptide coupling reactions, heterocyclic chemistry, and drug discovery, this product is rigorously tested for quality, ensuring consistent performance in sensitive applications. Available in various quantities, it is packaged under inert conditions to guarantee stability and longevity.

Properties

• CAS Number: 128293-64-1
• Complexity: 313
• IUPAC Name: 4-(tert-butoxycarbonylamino)-1-methyl-imidazole-2-carboxylic acid
• InChI: InChI=1S/C10H15N3O4/c1-10(2,3)17-9(16)12-6-5-13(4)7(11-6)8(14)15/h5H,1-4H3,(H,12,16)(H,14,15)
• InChI Key: GZBSJWBQXNCOFP-UHFFFAOYSA-N
• Exact Mass: 241.10625597
• Molecular Formula: C10H15N3O4
• Molecular Weight: 241.24
• SMILES: CC(C)(C)OC(=O)NC1=CN(C(=N1)C(=O)O)C
• Topological: 93.5
• Monoisotopic Mass: 241.10625597
• Synonyms: 128293-64-1, 4-(((1,1-Dimethylethoxy)carbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid, 4-[[(1,1-Dimethylethoxy)carbonyl]amino]-1-methyl-1H-imidazole-2-carboxylic acid, 4-((tert-Butoxycarbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid, 4-(boc-amino)-1-methyl-1h-imidazole-2-carboxylic acid, 4-tert-butoxycarbonylamino-1-methyl-1h-imidazole-2-carboxylic acid, 1-methyl-4-[(2-methylpropan-2-yl)oxycarbonylamino]imidazole-2-carboxylic Acid, MFCD03093495, 1H-IMIDAZOLE-2-CARBOXYLIC ACID, 4-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-1-METHYL-, 4-(tert-butoxycarbonylamino)-1-methyl-1H-imidazole-2-carboxylic acid, 4-{[(tert-butoxy)carbonyl]amino}-1-methylimidazole-2-carboxylic acid, 4-[(tert-butoxycarbonyl)amino]-1-methyl-1h-imidazole-2-carboxylic acid, SCHEMBL1986577, DTXSID40373780, GZBSJWBQXNCOFP-UHFFFAOYSA-N, 4-[(tert-butoxycarbonyl)amino]-1-methylimidazole-2-carboxylic acid, AKOS015902105, AB13245, CS-W021979, FD13122, AS-48891, SY063570, DB-041891, EN300-1071062, 1-methyl-4-(BOC amino)imidazole-2-carboxylic acid, (4-Boc-amino)-1-methyl-1H-imidazole-2-carboxylic acid, [(tert-butoxycarbonyl)amino]-1-methylimidazole-2-carboxylic acid, 4-[(t-butoxycarbonyl)amino]-1-methylimidazole-2-carboxylic acid, 4-tert-Butoxycarbonylamino-1-methyl-1H-imidazole -2-carboxylic acid, 4-[[(tert-Butyloxy)carbonyl]-amino]-1-methylimidazole-2-carboxylic acid, 4-{[(tert-butoxy)carbonyl]amino}-1-methyl-1H-imidazole-2-carboxylic acid

Application

This compound serves as a key intermediate in the synthesis of complex heterocycles and peptidomimetics, particularly in pharmaceutical research. Its Boc-protected amino group enables selective deprotection for further functionalization, while the carboxylic acid moiety allows for conjugation or derivatization. Researchers utilize it in the development of enzyme inhibitors, receptor modulators, and bioactive small molecules. Its stability and reactivity make it suitable for both solution-phase and solid-phase synthesis workflows.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (100%)
• Eye Irrit. 2 (100%)
• STOT SE 3 (100%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.