115576-91-5

Basic information

• Product Name: 1H-Benzimidazole-5-methanol,1-methyl-(9CI)
• Synonyms: 1H-Benzimidazole-5-methanol,1-methyl-(9CI);(1-Methyl-1H-benzo[d]imidazol-5-yl)methanol;(1-Methyl-1H-1,3-benzodiazol-5-yl)Methanol;(1-Methyl-1H-benzo[d]imidazol-5-yl);(1-methyl-1H-benzimidazol-5-yl)methanol
• CAS NO: 115576-91-5
• Molecular Formula: C9H10N2O
• Molecular Weight: 162.191
• Product Categories: BENZIMIDAZOLE
• Mol File: 115576-91-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 357.4°C at 760 mmHg
• Flash Point: 170°C
• Appearance: /
• Density: 1.22g/cm³
• Vapor Pressure: 9.92E-06mmHg at 25°C
• Refractive Index: 1.622
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1H-Benzimidazole-5-methanol,1-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazole-5-methanol,1-methyl-(9CI)(115576-91-5)
• EPA Substance Registry System: 1H-Benzimidazole-5-methanol,1-methyl-(9CI)(115576-91-5)

Safety Data

• Hazardous Substances Data: 115576-91-5(Hazardous Substances Data)

Usage

General Description

The chemical "1H-Benzimidazole-5-methanol, 1-methyl-(9CI)" is a specific type of organic compound that belongs to the family of benzimidazoles. Benzimidazoles are organic compounds that contain a benzene ring fused to an imidazole ring. It is a derivative of benzimidazole, substituted by a hydroxymethyl group at position 5 and a methyl group at the nitrogen atom. This substance is used in a variety of applications, however, detailed information about it, including its properties, uses, hazards, and safety measures, is not widely documented. Due to the absence of ample research, this chemical's behavior in the environment, long-term effects on the human body, and interactions with other chemicals are not accurately known.

InChI:InChI=1/C9H10N2O/c1-11-6-10-8-4-7(5-12)2-3-9(8)11/h2-4,6,12H,5H2,1H3

Upstream product

• 131020-36-5 methyl 1-methyl-1H-benzo[d]imidazole-5-carboxylate 
• 15788-16-6 5-benzimidazolecarboxylic acid 
• 26663-77-4 methyl 1H-benzo[d]imidazole-5-carboxylate 
• 71254-71-2 ethyl 4-(methylamino)-3-nitrobenzoate 
• 66315-23-9 ethyl 3-amino-4-(methylamino)benzoate 
• 53484-19-8 ethyl 1-methyl-1H-benzo[d]imidazole-5-carboxylate 
• 453-71-4 3-nitro-4-fluorobenzoic acid 
• 367-80-6 ethyl 4-fluoro-3-nitrobenzoate 

Downstream Products

• 279226-70-9 1-methyl-1H-benzo[d]imidazole-5-carbaldehyde 

Relevant articles and documents

HETEROCYCLIC COMPOUND AND p27Kip1 DEGRADATION INHIBITOR

A novel heterocyclic compound or a salt thereof useful for selectively inhibiting the degradation of p27Kip1 is provided. The compound or the salt thereof is represented by the following formula (1): wherein A represents an alkyl group, a cycloalkyl group, an aryl group or a heterocyclic group, the group A may have a substituent; the ring B represents a 5- to 8-membered monocyclic heterocyclic ring or a condensed ring containing the monocyclic heterocyclic ring, the ring B may have a substituent; the ring C represents an aromatic ring, the ring C may have a substituent; L represents a linker comprising a main chain having 3 to 5 atoms selected from the group consisting of a carbon atom, a nitrogen atom, an oxygen atom and a sulfur atom, wherein at least one atom in the main chain is a hetero atom selected from the group consisting of a nitrogen atom, an oxygen atom and a sulfur atom, the linker L may have a substituent; and n is 0 or 1.

CALCIUM RECEPTOR MODULATING AGENTS

The compounds of the invention are represented by the following general structure (I) or a pharmaceutically acceptable salt thereof, and compositions containing them, wherein the variables are defined herein, and their use to reduce or inhibit PTH secretion, including methods for reducing or inhibiting PTH secretion and methods for treatment or prophylaxis of diseases associated with bone disorders, such as osteoporosis, or associated with excessive secretion of PTH, such as hyperparathyroidism. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.