4-[(4-Bromobenzyl)amino]phenol

Base Information

Chemical Name:4-[(4-Bromobenzyl)amino]phenol
CAS No.:665015-09-8
Molecular Formula:C₁₃H₁₂BrNO
Molecular Weight:278.148
Hs Code.:
DSSTox Substance ID:DTXSID001283790
Mol file:665015-09-8.mol

Synonyms:4-[(4-bromobenzyl)amino]phenol;4-[(4-bromophenyl)methylamino]phenol;SCHEMBL14680444;BDBM453281;DTXSID001283790;HMS1617N21;STK285802;AKOS001696146;US10729695, Compound CB-14;CCG-315057;4-[[(4-Bromophenyl)methyl]amino]phenol;665015-09-8;AN-465/41673017

Suppliers and Price of 4-[(4-Bromobenzyl)amino]phenol

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 1 raw suppliers

Chemical Property of 4-[(4-Bromobenzyl)amino]phenol

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:277.01023
Heavy Atom Count:16
Complexity:196

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1CNC2=CC=C(C=C2)O)Br

Technology Process of 4-[(4-Bromobenzyl)amino]phenol

There total 3 articles about 4-[(4-Bromobenzyl)amino]phenol 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:

: 26213-37-6
4-(4-bromobenzylideneamino)phenol

: 665015-09-8
C₁₃H₁₂BrNO

Guidance literature:: With sodium tetrahydroborate; In methanol; at 20 ℃; for 1h;
DOI:10.1016/j.tet.2014.05.008

Reference yield:

: 123-30-8
4-amino-phenol

: 665015-09-8
C₁₃H₁₂BrNO

Guidance literature:: Multi-step reaction with 2 steps

1: methanol / 3 h / Reflux

2: sodium tetrahydroborate / methanol / 1 h / 20 °C

With sodium tetrahydroborate; In methanol;
DOI:10.1016/j.tet.2014.05.008

Reference yield:

: 1122-91-4
4-bromo-benzaldehyde

: 665015-09-8
C₁₃H₁₂BrNO

Guidance literature:: Multi-step reaction with 2 steps

1: methanol / 3 h / Reflux

2: sodium tetrahydroborate / methanol / 1 h / 20 °C

With sodium tetrahydroborate; In methanol;
DOI:10.1016/j.tet.2014.05.008