Isopropyldiphenylamine

Base Information

Chemical Name:Isopropyldiphenylamine
CAS No.:15541-77-2
Molecular Formula:C15H17N
Molecular Weight:211.307
Hs Code.:
ChEMBL ID:CHEMBL451157
DSSTox Substance ID:DTXSID20565585
Nikkaji Number:J1.872.710B
Wikidata:Q82450766
Mol file:15541-77-2.mol

Synonyms:isopropyldiphenylamine;15541-77-2;CHEMBL451157;SCHEMBL2119060;DTXSID20565585;N-Phenyl-N-(propan-2-yl)aniline

Suppliers and Price of Isopropyldiphenylamine

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 0 raw suppliers

Chemical Property of Isopropyldiphenylamine

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:211.136099547
Heavy Atom Count:16
Complexity:170

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Isopropyldiphenylamine

There total 10 articles about Isopropyldiphenylamine 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: 88.0%

: 108-86-1,52753-63-6
bromobenzene

: 768-52-5
N-Isopropylaniline

: 15541-77-2
N-iso-propyl-N-phenylaniline

Guidance literature:: With di-μ-bromobis(tri-tert-butylphosphino)dipalladium(I); sodium t-butanolate; In toluene; at 20 - 110 ℃;
DOI:10.1021/jo020609d

Reference yield: 77.0%

: 116-11-0
2-Methoxypropene

: 122-39-4
diphenylamine

: 15541-77-2
N-iso-propyl-N-phenylaniline

Guidance literature:: With sodium tris(acetoxy)borohydride; trifluoroacetic acid; In 1,2-dichloro-ethane; at 20 ℃; for 2h;
DOI:10.1055/s-2005-863704

Reference yield: 75.0%

: 122-39-4
diphenylamine

: 67-64-1
acetone

: 15541-77-2
N-iso-propyl-N-phenylaniline

Guidance literature:: With carbon monoxide; ruthenium(III) chloride trihydrate; In acetonitrile; at 160 ℃; for 48h; under 7600.51 - 38002.6 Torr; Reagent/catalyst; Solvent; Autoclave;
DOI:10.1039/c5cc08577b