4-[3-(Benzyloxy)phenyl]aniline

Base Information

Chemical Name:4-[3-(Benzyloxy)phenyl]aniline
CAS No.:400749-48-6
Molecular Formula:C19H17NO
Molecular Weight:275.34
Hs Code.:2922199090
DSSTox Substance ID:DTXSID20399822
Wikidata:Q82202580
Mol file:400749-48-6.mol

Synonyms:4-[3-(Benzyloxy)phenyl]aniline;400749-48-6;3'-(Benzyloxy)-[1,1'-biphenyl]-4-amine;4-(3-phenylmethoxyphenyl)aniline;3'-benzyloxybiphenyl-4-ylamine;SCHEMBL3786472;DTXSID20399822;MFCD04039052;AKOS004113303;3'-Benzyloxy[1,1-biphenyl]-4-amine;BS-28086;3'-(benzyloxy)[1,1'-biphenyl]-4-amine;BB 0222483;CS-0452223

Suppliers and Price of 4-[3-(Benzyloxy)phenyl]aniline

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

TRC
4-[3-(Benzyloxy)phenyl]aniline
100mg
$ 45.00

Crysdot
3'-(Benzyloxy)-[1,1'-biphenyl]-4-amine 95+%
10g
$ 564.00

Crysdot
3'-(Benzyloxy)-[1,1'-biphenyl]-4-amine 95+%
5g
$ 337.00

American Custom Chemicals Corporation
3'-BENZYLOXY[1,1-BIPHENYL]-4-AMINE 95.00%
1G
$ 1363.91

AK Scientific
4-[3-(Benzyloxy)phenyl]aniline
10g
$ 851.00

Total 10 raw suppliers

Chemical Property of 4-[3-(Benzyloxy)phenyl]aniline

Chemical Property:

PSA：35.25000
LogP:5.09600
Storage Temp.:2-8°C
XLogP3:4.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:275.131014166
Heavy Atom Count:21
Complexity:292

Purity/Quality:

97% ^*data from raw suppliers

4-[3-(Benzyloxy)phenyl]aniline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=CC=CC(=C2)C3=CC=C(C=C3)N

Technology Process of 4-[3-(Benzyloxy)phenyl]aniline

There total 2 articles about 4-[3-(Benzyloxy)phenyl]aniline 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:

: 156682-54-1
3-(benzyloxy)phenylboronic acid

: 540-37-4
p-aminoiodobenzene

: 400749-48-6
4-amino-3'-benzyloxybiphenyl

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; sodium carbonate; In 1,4-dioxane; water; Inert atmosphere; Reflux;
DOI:10.1016/j.bmcl.2015.04.038

Reference yield:

: 156682-54-1
3-(benzyloxy)phenylboronic acid

: 106-40-1
4-bromo-aniline

: 400749-48-6
4-amino-3'-benzyloxybiphenyl

Guidance literature:: With palladium 10% on activated carbon; tetrabutyl-ammonium chloride; sodium carbonate; In water; N,N-dimethyl-formamide; at 60 - 120 ℃; Microwave irradiation;
DOI:10.1016/j.bmcl.2009.02.073

Reference yield:

: 400749-48-6
4-amino-3'-benzyloxybiphenyl

: 90-02-8
salicylaldehyde

: 2-(((3'-(benzyloxy)-[1,1'-biphenyl]-4-yl)amino)methyl)phenol

Guidance literature:: 4-amino-3'-benzyloxybiphenyl; salicylaldehyde; In methanol; at 20 ℃; Inert atmosphere;

With sodium tetrahydroborate; In methanol; at 20 ℃; for 0.166667h; Inert atmosphere;
DOI:10.1016/j.bmcl.2015.04.038