1,2-Diamino-3,4,6-trifluorobenzene

Base Information

Chemical Name:1,2-Diamino-3,4,6-trifluorobenzene
CAS No.:363-74-6
Molecular Formula:C6H5F3N2
Molecular Weight:162.114
Hs Code.:
DSSTox Substance ID:DTXSID00344274
Nikkaji Number:J3.355.254H
Wikidata:Q82116006
Mol file:363-74-6.mol

Synonyms:3,4,6-trifluorobenzene-1,2-diamine;363-74-6;1,2-Diamino-3,4,6-trifluorobenzene;1,2-Benzenediamine, 3,4,6-trifluoro-;3,4,6-Trifluoro-1,2-benzenediamine;SCHEMBL859273;DTXSID00344274;AC9850;MFCD03001156;AKOS006276930;3,5,6-trifluoro-1,2-phenylenediamine;3,4,6-Trifluoro-1,2-benzenediamine #;SY263143

Suppliers and Price of 1,2-Diamino-3,4,6-trifluorobenzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 11 raw suppliers

Chemical Property of 1,2-Diamino-3,4,6-trifluorobenzene

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:0
Exact Mass:162.04048265
Heavy Atom Count:11
Complexity:144

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C(=C(C(=C1F)F)N)N)F
Use Description 1,2-Benzenediamine, 3,4,6-trifluoro-, is a chemical compound with diverse applications across various fields. In the realm of pharmaceuticals and medicinal chemistry, it can serve as a valuable intermediate for the synthesis of pharmaceutical agents and organic compounds, potentially contributing to the development of new drugs targeting a range of medical conditions. Its role is pivotal in drug discovery and development, aiding in the creation of medications with specific therapeutic properties. Additionally, in the field of materials science, 1,2-Benzenediamine, 3,4,6-trifluoro- can be employed as a precursor for the production of specialty polymers and organic materials with unique properties, contributing to advancements in materials technology. Furthermore, in the realm of chemical research and analytical chemistry, it may serve as a reference compound for the study of diamine derivatives and their reactivity, facilitating research in organic chemistry and chemical analysis. Its multifaceted utility underscores its significance in pharmaceuticals, materials science, and chemical research, where it plays a crucial role in drug innovation, material synthesis, and scientific investigation.

Technology Process of 1,2-Diamino-3,4,6-trifluorobenzene

There total 6 articles about 1,2-Diamino-3,4,6-trifluorobenzene 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: 87.0%

: 5415-62-3
2,3,5-trifluoro-6-nitroaniline

: 363-74-6
3,5,6-trifluoro-1,2-phenylenediamine

Guidance literature:: palladium; In ethanol;

Reference yield: 82.0%

: 132844-31-6,530102-90-0
4,5,7-Trifluoro-2,1,3-benzothiadiazole

: 363-74-6
3,5,6-trifluoro-1,2-phenylenediamine

Guidance literature:: With hydrogenchloride; tin(ll) chloride;
DOI:10.1016/S0022-1139(00)85001-0

Reference yield:

: 314-41-0
1,2,3,5-tetrafluoro-4-nitrobenzene

: 363-74-6
3,5,6-trifluoro-1,2-phenylenediamine

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / NH₃ / diethyl ether

2: 0.324 g / H₂ / Pd/C / ethanol

With ammonia; hydrogen; palladium on activated charcoal; In diethyl ether; ethanol;
DOI:10.1016/S0022-1139(00)82667-6