2-Phenyl-2H-benzotriazol-5-ylamine

Base Information

• Chemical Name: 2-Phenyl-2H-benzotriazol-5-ylamine
• CAS No.: 21819-66-9
• Molecular Formula: C12H10N4
• Molecular Weight: 210.238
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID50352208
• Nikkaji Number: J3.149.587C
• Wikidata: Q82129226
• ChEMBL ID: CHEMBL1410357
• Mol file: 21819-66-9.mol

Synonyms:2-Phenyl-2H-benzotriazol-5-ylamine;21819-66-9;2-phenylbenzotriazol-5-amine;2-phenyl-2h-benzo[d][1,2,3]triazol-5-amine;2-phenyl-2H-1,2,3-benzotriazol-5-amine;2-phenyl-2H-benzotriazol-5-amine;MLS000678352;SMR000285263;2-phenyl-2-hydrobenzotriazole-5-ylamine;2H-1,2,3-Benzotriazol-5-amine, 2-phenyl-;Cambridge id 5751857;TimTec1_000736;2-phenyl-5-benzotriazolamine;5-amino-2-phenylbenzotriazole;cid_721090;SCHEMBL1547419;CHEMBL1410357;BDBM43739;DTXSID50352208;(2-phenylbenzotriazol-5-yl)amine;NIOQXFRLZIIVCT-UHFFFAOYSA-N;HMS1536B10;HMS2631M18;KUC112598N;MFCD00179563;STK075616;AKOS000108466;CCG-106229;NCGC00175174-01;KSC-315-088-;2-phenyl-2H-1,2,3-benzotriazol-5-ylamine;BB 0245025;CS-0312876;AB00095784-01;AF-628/30886021;SR-01000430164;SR-01000430164-1;BRD-K62378038-001-01-4;Z57212893

Chemical Property of 2-Phenyl-2H-benzotriazol-5-ylamine

Chemical Property:

• PSA: 56.73000
• LogP: 2.58390
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 210.090546336
• Heavy Atom Count: 16
• Complexity: 239

Purity/Quality:

98%min ^*data from raw suppliers

2-phenyl-2H-benzo[d][1,2,3]triazol-5-amine ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)N2N=C3C=CC(=CC3=N2)N

Technology Process of 2-Phenyl-2H-benzotriazol-5-ylamine

There total 14 articles about 2-Phenyl-2H-benzotriazol-5-ylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.9%

2,4-diaminoazobenzene (495-54-5) → 2-phenyl-2H-benzo[d][1,2,3]triazol-5-amine (21819-66-9)

Guidance literature:

With pyridine; oxygen; copper(l) chloride; In ethanol; water; at 40 ℃;

DOI:10.1007/BF00949965

Reference yield: 85.0%

2-phenyl-5-nitrobenzotriazole (64264-33-1) → 2-phenyl-2H-benzo[d][1,2,3]triazol-5-amine (21819-66-9)

Guidance literature:

With hydrogenchloride; tin(ll) chloride; In N,N-dimethyl-formamide;

DOI:10.1007/BF00478859

Reference yield: 77.0%

Basic orange 2 (532-82-1) → 2-phenyl-2H-benzo[d][1,2,3]triazol-5-amine (21819-66-9)

Guidance literature:

With ammonium hydroxide; copper(ll) sulfate pentahydrate; In ethanol; water; for 4h; Reflux;

DOI:10.1016/j.tet.2011.01.026

upstream raw materials:

3-nitro-4-phenylazo-aniline

2,4-diaminoazobenzene

2-phenyl-5-nitrobenzotriazole

ethanol

Downstream raw materials:

2-phenyl-2H-[1,2,3]triazolo[4,5-f]quinoline

2-phenyl-2H-1,2,3-benzotriazole

2-phenyl-5-hydroxybenzotriazole

2-phenyl-1,2,3-triazole-4,5-dicarboxylic acid