3-Phenyl-p-anisidine

Base Information

Chemical Name:3-Phenyl-p-anisidine
CAS No.:56970-26-4
Molecular Formula:C13H13NO
Molecular Weight:199.25
Hs Code.:
European Community (EC) Number:834-037-6
DSSTox Substance ID:DTXSID80972438
Wikidata:Q72501263

Synonyms:56970-26-4;3-Phenyl-p-anisidine;4-methoxy-3-phenylaniline;5-Amino-2-methoxybiphenyl;6-Methoxy(1,1'-biphenyl)-3-amine;6-Methoxy[1,1'-biphenyl]-3-amine;6-methoxy-[1,1'-biphenyl]-3-amine;(1,1'-Biphenyl)-3-amine, 6-methoxy-;4-methoxy-3-phenyl aniline;6-methoxybiphenyl-3-ylamine;SCHEMBL654302;DTXSID80972438;AKOS006281197;6-Methoxy[1,1'-biphenyl]-3-amine #;FT-0657435;EN300-255745;A1-66382;Z1198163387

Suppliers and Price of 3-Phenyl-p-anisidine

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

American Custom Chemicals Corporation
3-PHENYL-4-ANISIDINE 95.00%
5G
$ 909.56

AK Scientific
3-Phenyl-p-anisidine
100mg
$ 162.00

Total 9 raw suppliers

Chemical Property of 3-Phenyl-p-anisidine

Chemical Property:

Vapor Pressure:8.78E-05mmHg at 25°C
Refractive Index:1.598
Boiling Point:340.1 °C at 760 mmHg
PKA:4.94±0.10(Predicted)
Flash Point:166.2 °C
PSA：35.25000
Density:1.1 g/cm³
LogP:3.52560
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:199.099714038
Heavy Atom Count:15
Complexity:189

Purity/Quality:

98%min ^*data from raw suppliers

3-PHENYL-4-ANISIDINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)N)C2=CC=CC=C2

Technology Process of 3-Phenyl-p-anisidine

There total 8 articles about 3-Phenyl-p-anisidine 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:

: 15854-75-8
2-methoxy-5-nitro-1,1’-biphenyl

: 56970-26-4
6-methoxy-[1,1’-biphenyl]-3-amine

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00341a020

Reference yield:

: 79380-81-7
2-methoxy-5-(phenylazo)biphenyl

: 56970-26-4
6-methoxy-[1,1’-biphenyl]-3-amine

Guidance literature:: With ethanol; nickel; at 100 ℃; under 92673.9 Torr; Hydrogenation;
DOI:10.1021/ja01212a047

Reference yield:

: 132-27-4
sodium 2-biphenylate

: 56970-26-4
6-methoxy-[1,1’-biphenyl]-3-amine

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) aq. HCl, NaNO₂ / 1.) 0 deg C, 2.) 0-2 deg C

2: 1.) NaH / 1.) DMF, from RT to 70 deg C, 2.) DMF, 70 deg C, 2 h

3: 2.3 g / H₂ / 10percent Pd/C / ethanol / 760 Torr

With hydrogenchloride; hydrogen; sodium hydride; sodium nitrite; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00144a019