4-bromo-N-ethylaniline

Base Information

Chemical Name:4-bromo-N-ethylaniline
CAS No.:68254-64-8
Molecular Formula:C8H10BrN
Molecular Weight:200.078
Hs Code.:
European Community (EC) Number:827-786-5
DSSTox Substance ID:DTXSID30471704
Nikkaji Number:J730.132D
Wikidata:Q82300348

Synonyms:4-bromo-N-ethylaniline;68254-64-8;Benzenamine, 4-bromo-N-ethyl-;N-Ethyl-4-bromo-benzenamine;4-bromo-N-ethylbenzenamine;N-ethyl-4-bromoaniline;SCHEMBL1284249;DTXSID30471704;VYSQUDVPQJEULO-UHFFFAOYSA-N;AKOS000241185;SB77025;CS-0246453;EN300-32929;F78853;Z286365048

Suppliers and Price of 4-bromo-N-ethylaniline

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 5 raw suppliers

Chemical Property of 4-bromo-N-ethylaniline

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:198.99966
Heavy Atom Count:10
Complexity:87.3

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCNC1=CC=C(C=C1)Br

Technology Process of 4-bromo-N-ethylaniline

There total 20 articles about 4-bromo-N-ethylaniline 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: 96.0%

: 103-88-8
4-bromoacetanilide

: 68254-64-8
4-bromo-N-ethylaniline

Guidance literature:: With dimethylsulfide borane complex; In tetrahydrofuran; at 90 ℃; for 0.333333h; under 7500.75 Torr; chemoselective reaction; Inert atmosphere; Flow reactor;
DOI:10.1002/cssc.201903459

Reference yield: 89.0%

: 554-68-7
triethylamine hydrochloride

: 121-44-8
triethylamine

: 106-40-1
4-bromo-aniline

: 68254-64-8
4-bromo-N-ethylaniline

Guidance literature:: With [Cp*IrCl(C₅H₄CH₂C₅H₃OH)][Cl]; In methanol; at 120 ℃; for 12h; Schlenk technique;
DOI:10.1021/acs.organomet.9b00172

Reference yield: 86.0%

: 64-19-7,77671-22-8
acetic acid

: 106-40-1
4-bromo-aniline

: 68254-64-8
4-bromo-N-ethylaniline

Guidance literature:: With C₂₅H₄₂N₆Rh⁽¹⁺⁾*CF₃O₃S^(1-); phenylsilane; In tetrahydrofuran; at 30 ℃; for 20h; Inert atmosphere;
DOI:10.1002/adsc.201500875