2,6-Dichloro-4-trifluoromethylphenylazide

Base Information

• Chemical Name: 2,6-Dichloro-4-trifluoromethylphenylazide
• CAS No.: 133152-04-2
• Molecular Formula: C₇H₂Cl₂F₃N₃
• Molecular Weight: 256.014
• DSSTox Substance ID: DTXSID20599825
• Wikidata: Q82495782

Synonyms:133152-04-2;2,6-DICHLORO-4-TRIFLUOROMETHYLPHENYLAZIDE;2-azido-1,3-dichloro-5-(trifluoromethyl)benzene;Benzene, 2-azido-1,3-dichloro-5-(trifluoromethyl)-;2,6-Dichloro-4-(trifluoromethyl)phenylazide;DTXSID20599825;MFCD12406795;2,6-dichloro-4-trifluoromethylphenyl azide;1-azido-2,6-dichloro-4-trifluoromethylbenzene;G38003;EN300-9455943

Chemical Property of 2,6-Dichloro-4-trifluoromethylphenylazide

Chemical Property:

• XLogP3: 5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 254.9577870
• Heavy Atom Count: 15
• Complexity: 265

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C=C(C(=C1Cl)N=[N+]=[N-])Cl)C(F)(F)F

Technology Process of 2,6-Dichloro-4-trifluoromethylphenylazide

There total 1 articles about 2,6-Dichloro-4-trifluoromethylphenylazide 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: 95.0%

2,6-dichloro-4-(trifluoromethyl)aniline (24279-39-8) → 2-azido-1,3-dichloro-5-(trifluoromethyl)benzene (133152-04-2)

Guidance literature:

2,6-dichloro-4-(trifluoromethyl)aniline; With hydrogenchloride; sodium nitrite; at 0 ℃; for 2h;

With sodium azide; sodium acetate; In water; Further stages.;

DOI:10.3390/molecules13030556

Reference yield: 99.0%

2-azido-1,3-dichloro-5-(trifluoromethyl)benzene (133152-04-2) + phenylacetylene (536-74-3) → 1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-phenyl-1H-[1,2,3]triazole

Guidance literature:

With copper(II) sulfate; sodium L-ascorbate; In tert-butyl alcohol;

DOI:10.1021/jf052773i

Reference yield: 91.0%

2-azido-1,3-dichloro-5-(trifluoromethyl)benzene (133152-04-2) + hex-1-yne (693-02-7) → 4-butyl-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-[1,2,3]triazole

Guidance literature:

With copper(l) iodide; N-ethyl-N,N-diisopropylamine; at 25 ℃; for 16h;

DOI:10.3390/molecules13030556

upstream raw materials:

2,6-dichloro-4-(trifluoromethyl)aniline

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