(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol

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CAS:103755-58-4
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CAS:103755-58-4

(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol manufacturers

(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol Basic information
Product Name:(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol
Synonyms:(1-PHENYL-1H-1,2,3-TRIAZOL-4-YL)METHANOL;1-Phenyl-1H-1,2,3-Triazol-4-yl;(1-phenyl-1H-1,2,3-triazole-4-yl)methanol;1H-1,2,3-Triazole-4-methanol, 1-phenyl-;1-Phenyl-1H-1,2,3-triazole-4-methanol, 97%
CAS:103755-58-4
MF:C9H9N3O
MW:175.19
EINECS:
Product Categories:API intermediates;Pyrrodiazole;Heterocyclic Series
Mol File:103755-58-4.mol
(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol Structure
(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol Chemical Properties
Melting point 114-116°C
Boiling point 379.9±34.0 °C(Predicted)
density 1.27±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka12.96±0.10(Predicted)
CAS DataBase Reference103755-58-4(CAS DataBase Reference)
Safety Information
HazardClass IRRITANT
HS Code 2933998090
MSDS Information
(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol Usage And Synthesis
Synthesis
Propargyl alcohol

107-19-7

PHENYL AZIDE

622-37-7

(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol

103755-58-4

General procedure: Azidobenzene (1 eq.), 2-propyn-1-ol (1.5 eq.) and copper sulfate pentahydrate (0.1 eq.) were dissolved in a solvent mixture of water and acetonitrile (12 mL, water:acetonitrile = 2:1, v/v) at room temperature. Hydrazine hydrate (1 eq.) was added dropwise to the above solution under vigorous stirring. The reaction mixture gradually changed to light yellow or light green color. The progress of the reaction is monitored by thin layer chromatography (TLC) and the reaction is usually completed within a few minutes (see Table 3 for specific times). Upon completion of the reaction, the product usually precipitates as a colorless solid (unless otherwise noted). The reaction mixture is diluted with excess water and subsequently filtered. The collected solid product is washed with water and dried. The resulting solid may be crystallized by dissolution in a suitable solvent or filtered through a pad of diatomaceous earth to obtain analytically pure 1-phenyl-1hydro-4-methanolyl-1,2,3-triazole.

References[1] New Journal of Chemistry, 2006, vol. 30, # 8, p. 1137 - 1139
[2] Green Chemistry, 2012, vol. 14, # 5, p. 1298 - 1301
[3] Applied Catalysis A: General, 2013, vol. 453, p. 151 - 158
[4] Archiv der Pharmazie, 2015, vol. 348, # 11, p. 796 - 807
[5] New Journal of Chemistry, 2015, vol. 39, # 8, p. 5902 - 5907
Tag:(1-Phenyl-1H-1,2,3-triazol-4-yl)methanol(103755-58-4) Related Product Information
Diphenyl ether 2-Phenylphenol Triphenylphosphine oxide Triton X-100 PHENYL VALERATE Methanol Triphenylphosphine Phenyl salicylate PHENYL RESIN [1-(4-Chlorophenyl)-1H-1,2,3-triazol-4-yl]methanol Phenylacetone Phenylacetic acid 5-METHYL-1-[3-(TRIFLUOROMETHYL)PHENYL]-1H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID (5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOL-4-YL)METHANOL METHYL 5-(2-METHOXY-2-OXOETHYL)-1-(4-METHOXYPHENYL)-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE METHYL 1-(2,4-DICHLOROPHENYL)-5-(2-METHOXY-2-OXOETHYL)-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE METHYL 1-(4-CHLOROPHENYL)-5-(2-METHOXY-2-OXOETHYL)-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE METHYL 5-(2-METHOXY-2-OXOETHYL)-1-[3-(TRIFLUOROMETHYL)PHENYL]-1H-1,2,3-TRIAZOLE-4-CARBOXYLATE

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