84440-19-7

Basic information

• Product Name: 1H-1,2,3-TRIAZOLE-4-METHANOL
• Synonyms: 1H-1,2,3-TRIAZOLE-4-METHANOL;1H-1,2,3-Triazole-5-Methanol;(1H-1,2,3-Triazol-4-yl)Methanol;(2H-1,2,3-triazol-4-yl)methanol;2H-1,2,3-triazol-4-ylmethanol;2H-triazol-4-ylmethanol
• CAS NO: 84440-19-7
• Molecular Formula: C3H5N3O
• Molecular Weight: 99.09
• Mol File: 84440-19-7.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 346.5°C at 760 mmHg
• Flash Point: 163.4°C
• Appearance: /
• Density: 1.456g/cm³
• Vapor Pressure: 2.17E-05mmHg at 25°C
• Refractive Index: 1.601
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1H-1,2,3-TRIAZOLE-4-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,3-TRIAZOLE-4-METHANOL(84440-19-7)
• EPA Substance Registry System: 1H-1,2,3-TRIAZOLE-4-METHANOL(84440-19-7)

Safety Data

• Hazardous Substances Data: 84440-19-7(Hazardous Substances Data)

Usage

General Description

1H-1,2,3-Triazole-4-methanol, also known as 2-Amino-1,2,3-triazole-4-methanol, is a chemical compound with the molecular formula C2H4N4O. It is a derivative of triazole and is used in the production of various pharmaceuticals, including antiviral and anticancer drugs. 1H-1,2,3-Triazole-4-methanol has also shown potential as a corrosion inhibitor in the petroleum industry and as a ligand in coordination chemistry. Additionally, it has been studied for its potential antimicrobial and antifungal properties, making it a versatile and valuable compound in various fields of research and application.

InChI:InChI=1/C3H5N3O/c7-2-3-1-4-6-5-3/h1,7H,2H2,(H,4,5,6)

Upstream product

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Relevant articles and documents

SUBSTITUTED NITROGEN CONTAINING COMPOUNDS

Disclosed are compounds of Formula (I): or a salt thereof, Formula (II) wherein R1 is: or; each W is independently NR1b or O; Z is a bond or CHR1d; and R1, R2, Rd, R3a, R3b, L1, B, V, Y, and n are defined herein. Also disclosed are methods of using such compounds as inhibitors of ROMK, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating cardiovascular diseases.

Investigation of copper-free alkyne/azide 1,3-dipolar cycloadditions using microwave irradiation

The prevalence of 1,3-dipolar cycloadditions of azides and alkynes within both biology and chemistry highlights the utility of these reactions. However, the use of a copper catalyst can be prohibitive to some applications. Consequently, we have optimized

MONOBACTAM ORGANIC COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS

This invention pertains generally to antibacterial compounds of Formula I, as further described herein, and pharmaceutically acceptable salts and formulations thereof. In certain aspects, the invention pertains to methods of using such compounds to treat infections such as those caused by Gram-negative bacteria.