Description

2-Chloro-1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole (CAS: 1315281-29-8) is a high-purity boronic ester derivative, extensively utilized in pharmaceutical research and organic synthesis. With the molecular formula C₁₀H₁₆BClN₂O₂, this compound serves as a versatile intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex heterocyclic frameworks. Its pinacol boronate ester group ensures enhanced stability and reactivity, making it ideal for precision chemical transformations. Suitable for laboratory-scale applications, this product is rigorously tested for purity and consistency, ensuring reliable performance in synthetic workflows. Store under inert conditions to maintain stability.

Properties

• CAS Number: 1315281-29-8
• Complexity: 272
• IUPAC Name: 2-chloro-1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazole
• InChI: InChI=1S/C10H16BClN2O2/c1-9(2)10(3,4)16-11(15-9)7-6-13-8(12)14(7)5/h6H,1-5H3
• InChI Key: MOQXZCYTVMKINQ-UHFFFAOYSA-N
• Exact Mass: 242.0993356
• Molecular Formula: C10H16BClN2O2
• Molecular Weight: 242.51
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CN=C(N2C)Cl
• Topological: 36.3
• Monoisotopic Mass: 242.0993356
• Synonyms: 1315281-29-8, 2-Chloro-1-methylimidazole-5-boronic Acid Pinacol Ester, 2-Chloro-1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole, 2-chloro-1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazole, 1H-Imidazole, 2-chloro-1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, MFCD11100959, (2-CHLORO-1-METHYL-1H-IMIDAZOL-5-YL)BORONIC ACID PINACOL ESTER, MOQXZCYTVMKINQ-UHFFFAOYSA-N, CHEMBL3236901, SCHEMBL15209118, 2-CHLORO-1-METHYL-1H-IMIDAZOLE-5-BORONIC ACID PINACOL ESTER, 2-chloro-1-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole, AKOS022183133, AS-32534, SY013201, CS-0061113, EN300-298557, Z2044824082

This compound is widely employed as a key intermediate in the synthesis of bioactive molecules and pharmaceuticals, particularly in the development of imidazole-based drug candidates. Its boronate ester functionality facilitates efficient cross-coupling reactions, enabling the introduction of imidazole motifs into complex molecular architectures. Researchers leverage its reactivity for constructing novel heterocyclic compounds in medicinal chemistry and materials science. Ideal for use under controlled conditions in inert atmospheres to prevent degradation.

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