103755-58-4

103755-58-4 - Names and Identifiers

Name	(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol
Synonyms	1-Phenyl-1H-1,2,3-Triazol-4-yl 1-phenyl-1H-1,2,3-triazol-4-yl methanol 1H-1,2,3-Triazole-4-methanol, 1-phenyl- (1-Phenyl-1H-1,2,3-triazol-4-yl)methanol (1-PHENYL-1H-1,2,3-TRIAZOL-4-YL)METHANOL (1-phenyl-1H-1,2,3-triazole-4-yl)methanol
CAS	103755-58-4
InChI	InChI=1/C9H9N3O/c13-7-8-6-12(11-10-8)9-4-2-1-3-5-9/h1-6,13H,7H2

103755-58-4 - Physico-chemical Properties

Molecular Formula	C9H9N3O
Molar Mass	175.19
Density	1.27±0.1 g/cm3(Predicted)
Melting Point	114-116°C
Boling Point	379.9±34.0 °C(Predicted)
Flash Point	183.6°C
Vapor Presure	1.9E-06mmHg at 25°C
pKa	12.96±0.10(Predicted)
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.642

103755-58-4 - Risk and Safety

Hazard Class

IRRITANT

103755-58-4 - Introduction

1-Phenyl-4-carbinolyl-1H-1, 2,3-triazole is an organic compound. Its structure contains a benzene ring and a triazole ring, in which the 4-methanol group is attached to the benzene ring. The following is a description of some of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance: A colorless to pale yellow solid.
-Solubility: Soluble in some organic solvents, such as ethanol and dichloromethane.
-Melting point: about 60-63°C.
-Stability: relatively stable under normal conditions.

Use:
- 1-phenyl -4-carbinol -1H-1,2,3-triazole can be used as an organic synthesis intermediate, involved in the synthesis of various organic compounds.
-It can also be used as a ligand for organic catalysts to promote organic reactions.

Preparation Method:
-1-Phenyl-4-carbinyl-1H-1, 2,3-triazole can be obtained by reacting phenylboronic acid with 3-amino -1,2,4-triazole in the presence of a catalyst.
-The specific preparation method may require more detailed experimental conditions and steps.

Safety Information:
-As no specific safety data is available, standard laboratory safety measures should be taken when using the compound, including wearing appropriate personal protective equipment (such as gloves and protective glasses).
-This compound may be irritating to the eyes, skin and respiratory tract. Therefore, avoid contact with skin and eyes when using, and prevent inhalation of its aerosol.
-During handling and storage, avoid contact with oxidants and strong acids, and keep away from fire sources.

Please note that the information here is only a general description of the compound. Specific properties and safety information may require reference to more specific literature and laboratory guidance. Always follow laboratory safety practices when operating chemical experiments.

Last Update：2024-04-09 21:04:16