Biphenyl-2-carboxamidine

Base Information

Chemical Name:Biphenyl-2-carboxamidine
CAS No.:175692-06-5
Molecular Formula:C13H12 N2
Molecular Weight:196.25
Hs Code.:2925290090
Nikkaji Number:J723.833I
Mol file:175692-06-5.mol

Synonyms:Biphenyl-2-carboxamidine;175692-06-5;2-phenylbenzenecarboximidamide;[1,1'-Biphenyl]-2-carboximidamide;2-phenylbenzene-1-carboximidamide;o-Phenylbenzamidine;2-phenylbenzamidine;biphenyl-2-carboximidamide;SCHEMBL1034554;1,1'-Biphenyl-2-carboxamidine;LNUYLGUBVHEHEL-UHFFFAOYSA-N;AKOS006293460;FT-0691565;EN300-1863503

Suppliers and Price of Biphenyl-2-carboxamidine

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
BIPHENYL-2-CARBOXAMIDINE 95.00%
5MG
$ 499.53

Total 4 raw suppliers

Chemical Property of Biphenyl-2-carboxamidine

Chemical Property:

Vapor Pressure:2.35E-06mmHg at 25°C
Boiling Point:386.6°Cat760mmHg
Flash Point:187.6°C
PSA：49.87000
Density:g/cm³
LogP:3.43770
XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:196.100048391
Heavy Atom Count:15
Complexity:219

Purity/Quality:

97% ^*data from raw suppliers

BIPHENYL-2-CARBOXAMIDINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC=CC=C2C(=N)N

Technology Process of Biphenyl-2-carboxamidine

There total 3 articles about Biphenyl-2-carboxamidine 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: 79.0%

: 24973-49-7
biphenyl-2-carbonitrile

: 175692-06-5
<1,1'>-biphenyl-2-carbamidine

Guidance literature:: With trimethylaluminum; ammonium chloride; In toluene; for 15h; Reflux;

Reference yield:

: 2042-37-7
o-cyanobromobenzene

: 175692-06-5
<1,1'>-biphenyl-2-carbamidine

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / 2 M aq. Na₂CO₃ / Pd(PPh₃)4 / toluene; ethanol / 16 h / Heating

2: 57 percent / 0.67 M MeAlClNH₂ / methanol; toluene / 20 h / 90 °C

With amino(methyl)aluminum chloride; sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In methanol; ethanol; toluene;
DOI:10.1002/ardp.19963290204

Reference yield:

: 98-80-6
phenylboronic acid

: 175692-06-5
<1,1'>-biphenyl-2-carbamidine

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / 2 M aq. Na₂CO₃ / Pd(PPh₃)4 / toluene; ethanol / 16 h / Heating

2: 57 percent / 0.67 M MeAlClNH₂ / methanol; toluene / 20 h / 90 °C

With amino(methyl)aluminum chloride; sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In methanol; ethanol; toluene;
DOI:10.1002/ardp.19963290204