1H-Imidazole-4-methanol, α-methyl-, monohydrochloride, with the CAS number 62256-53-5, is a chemical compound that features an imidazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. This compound is characterized by the presence of a hydroxymethyl group (-CH2OH) and an α-methyl group, which contributes to its unique properties. As a hydrochloride salt, it is typically encountered in a solid form, which enhances its stability and solubility in water. The imidazole moiety is known for its biological significance, often acting as a building block in various pharmaceuticals and biochemical applications. The compound may exhibit properties such as being a weak base due to the nitrogen atoms in the ring, and it can participate in hydrogen bonding due to the hydroxymethyl group. Its potential applications may include roles in medicinal chemistry, particularly in the development of drugs targeting various biological pathways. Overall, this compound is of interest in both synthetic and medicinal chemistry contexts.

1H-Imidazole-4-methanol, a-methyl-, monohydrochloride

62256-53-5: 1H-Imidazole-4-methanol, α-methyl-, monohydrochloride, with the CAS number 62256-53-5, is a chemical compound that features an imidazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms. This compound is characterized by the presence of a hydroxymethyl group (-CH2OH) and an α-methyl group, which contributes to its unique properties. As a hydrochloride salt, it is typically encountered in a solid form, which enhances its stability and solubility in water. The imidazole moiety is known for its biological significance, often acting as a building block in various pharmaceuticals and biochemical applications. The compound may exhibit properties such as being a weak base due to the nitrogen atoms in the ring, and it can participate in hydrogen bonding due to the hydroxymethyl group. Its potential applications may include roles in medicinal chemistry, particularly in the development of drugs targeting various biological pathways. Overall, this compound is of interest in both synthetic and medicinal chemistry contexts.

CAS 62256-53-5

1H-Imidazole-4-methanol, a-methyl-, monohydrochloride

1-(1H-IMIDAZOL-4-YL)-ETHANOL HCL

Ref: IN-DA00EFJK

1-(1H-IMIDAZOL-4-YL)-ETHANOL HCL

Ref: 10-F468939

1-(1H-Imidazol-4-yl)ethanol Hydrochloride

Ref: 3D-MCA25653