188956
4-Phenylurazole
98%
Synonym(s):
4-Phenyl-1,2,4-triazolidine-3,5-dione, Ph-Ur for e-Y-CLICK
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25 G
€81.50
About This Item
Empirical Formula (Hill Notation):
C8H7N3O2
CAS Number:
Molecular Weight:
177.16
Beilstein:
163361
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
mp
207-209 °C (lit.)
SMILES string
O=C1NNC(=O)N1c2ccccc2
InChI
1S/C8H7N3O2/c12-7-9-10-8(13)11(7)6-4-2-1-3-5-6/h1-5H,(H,9,12)(H,10,13)
InChI key
GOSUFRDROXZXLN-UHFFFAOYSA-N
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General description
4-Phenylurazole undergoes oxidation in the presence of NO2-N2O4 to yield 4-phenyl-1,2,4-trizoline-3,5-dione[1]. It undergoes acetylation reaction with excess acetyl chloride in N,N-dimethylacetamide solution[2]. It polymerizes in the presence of phosgene, terephthaloyl chloride and epichlorohydrin to yield insoluble polymer[3]. It is precursor to the Diels-Alder trapping agent, 4-phenyl-1,2,4-triazoline-3,5-dione[4][5][6]. This urazole was recently demonstrated in the traceless, chemoselective labeling of peptides and proteins through electrochemical tyrosine-click (e-Y-CLICK) chemistry.
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Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Polycondensation Reaction of 4-(4'-N-1, 8-Naphthalimidophenyl)-1, 2, 4-triazolidine-3, 5-dione with Aliphatic Diacid Chlorides.
Mallakpour S and Rafiee Z.
Iranian Polymer Journal, 13, 225-234 (2004)
Chemische Berichte, 121, 185-185 (1988)
Journal of the American Chemical Society, 109, 3730-3730 (1987)
A new method for the oxidation of 4-phenylurazole to 4-phenyltriazolinedione.
Mallakpour SE.
Journal of Chemical Education, 69(3), 238-238 (1992)
Bulletin of the Chemical Society of Japan, 61, 3915-3915 (1988)
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