N-(Phenylmethyl)[1,1-biphenyl]-2-amine

Base Information Edit

Chemical Name:N-(Phenylmethyl)[1,1-biphenyl]-2-amine
CAS No.:52648-48-3
Molecular Formula:C₁₉H₁₇N
Molecular Weight:259.351
Hs Code.:
DSSTox Substance ID:DTXSID901277998
Nikkaji Number:J2.406.409C
Mol file:52648-48-3.mol

Synonyms:52648-48-3;DTXSID901277998;AKOS009069568;N-(Phenylmethyl)[1,1-biphenyl]-2-amine;N-(Phenylmethyl)[1,1'-biphenyl]-2-amine

Suppliers and Price of N-(Phenylmethyl)[1,1-biphenyl]-2-amine

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(Phenylmethyl)[1,1-biphenyl]-2-amine Edit

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:259.136099547
Heavy Atom Count:20
Complexity:263

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC2=CC=CC=C2C3=CC=CC=C3

Technology Process of N-(Phenylmethyl)[1,1-biphenyl]-2-amine

There total 17 articles about N-(Phenylmethyl)[1,1-biphenyl]-2-amine 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: 99.0%

: 86-00-0
2-nitrobiphenyl

: 100-51-6,185532-71-2
benzyl alcohol

: 52648-48-3
N-(phenylmethyl)-(1,1'-biphenyl)-2-amine

Guidance literature:: With Au/Fe₂O₃; at 160 ℃; for 19h; chemoselective reaction; Inert atmosphere;
DOI:10.1039/c1cc11057h

Reference yield: 93.0%

: 90-41-5
2-phenylaniline

: 100-51-6,185532-71-2
benzyl alcohol

: 52648-48-3
N-(phenylmethyl)-(1,1'-biphenyl)-2-amine

Guidance literature:: With [(η5-pentamethylcyclopentadienyl)Ir^IIIbis-(κC-1,3-dimethylimidazol-2-ylidene)Cl]BF₄; potassium tert-butylate; In toluene; at 80 ℃; for 12h;
DOI:10.1016/j.poly.2021.115289

Reference yield: 93.0%

: 52648-48-3
N-(phenylmethyl)-(1,1'-biphenyl)-2-amine

Guidance literature:: With potassium tert-butylate; molybdenum hexacarbonyl; 1,1'-dimethyl-3,3'-methylenediimidazolium bromide; In hexane; at 130 ℃; for 24h; Schlenk technique; Inert atmosphere;