3,5-Dibromo-4-ethoxyaniline

Base Information

Chemical Name:3,5-Dibromo-4-ethoxyaniline
CAS No.:52765-17-0
Molecular Formula:C₈H₉Br₂NO
Molecular Weight:294.974
Hs Code.:
DSSTox Substance ID:DTXSID60655914
Wikidata:Q82570290
Mol file:52765-17-0.mol

Synonyms:3,5-Dibromo-4-ethoxyaniline;52765-17-0;Benzenamine, 3,5-dibromo-4-ethoxy-;SCHEMBL1457731;DTXSID60655914;RVAIEOIDJDTMJC-UHFFFAOYSA-N;A1-39900

Suppliers and Price of 3,5-Dibromo-4-ethoxyaniline

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
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price

Total 0 raw suppliers

Chemical Property of 3,5-Dibromo-4-ethoxyaniline

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:294.90304
Heavy Atom Count:12
Complexity:133

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=C(C=C(C=C1Br)N)Br

Technology Process of 3,5-Dibromo-4-ethoxyaniline

There total 4 articles about 3,5-Dibromo-4-ethoxyaniline 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:

: 31106-76-0
2,6-dibromo-4-nitro-phenetole

: 52765-17-0
4-ethoxy-3,5-dibromo-aniline

Guidance literature:: With sodium sulfide; ethanol; sulfur;

Reference yield:

: 99-28-5
2,6-dibromo-4-nitrophenol

: 52765-17-0
4-ethoxy-3,5-dibromo-aniline

Guidance literature:: Multi-step reaction with 3 steps

1: sodium dithionite

3: potassium hydroxide; ethanol / Erhitzen des Reaktionsprodukts mit wss. Salzsaeure

With potassium hydroxide; sodium dithionite; ethanol;

Reference yield:

: 3460-20-6
1,2,3-tribromo-5-nitrobenzene

: 52765-17-0
4-ethoxy-3,5-dibromo-aniline

Guidance literature:: Multi-step reaction with 2 steps

2: tin dichloride; hydrochloric acid

With hydrogenchloride; tin(ll) chloride;