N-Benzyl-4-iodoaniline

Base Information

Chemical Name:N-Benzyl-4-iodoaniline
CAS No.:3526-49-6
Molecular Formula:C13H12 I N
Molecular Weight:309.149
Hs Code.:2921420090
ChEMBL ID:CHEMBL2296110
DSSTox Substance ID:DTXSID20565843
Nikkaji Number:J2.545.854K
Wikidata:Q82451145
Mol file:3526-49-6.mol

Synonyms:N-BENZYL-4-IODOANILINE;3526-49-6;BENZYL-(4-IODO-PHENYL)-AMINE;Benzenemethanamine,N-(4-iodophenyl)-;CHEMBL2296110;N-benzyl-p-iodoaniline;SCHEMBL4513303;DTXSID20565843;XRLJKIYWSQACLG-UHFFFAOYSA-N;N-(4-Iodophenyl)benzenemethanamine;BDBM50489090;MFCD09033515;AKOS009061180;A1-05496

Suppliers and Price of N-Benzyl-4-iodoaniline

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

Matrix Scientific
N-Benzyl-4-iodoaniline 95%
5g
$ 990.00

A1 Biochem Labs
N-benzyl-4-iodoaniline 95%
5 g
$ 600.00

Total 7 raw suppliers

Chemical Property of N-Benzyl-4-iodoaniline

Chemical Property:

PSA：12.03000
LogP:3.97630
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:309.00145
Heavy Atom Count:15
Complexity:169

Purity/Quality:

99% ^*data from raw suppliers

N-Benzyl-4-iodoaniline 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC2=CC=C(C=C2)I

Technology Process of N-Benzyl-4-iodoaniline

There total 20 articles about N-Benzyl-4-iodoaniline 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%

: 100-52-7
benzaldehyde

: 540-37-4
p-aminoiodobenzene

: 3526-49-6
N-(4-iodophenyl)benzylamine

Guidance literature:: With (2,6-dichlorophenyl)bis(2,3,5,6-tetrafluorophenyl)borane; hydrogen; In tetrahydrofuran; at 100 ℃; for 6h; under 15201 Torr; Sealed tube; Molecular sieve; Autoclave; Green chemistry;
DOI:10.1021/jacs.8b03626

Reference yield: 99.0%

: 3381-47-3,102904-39-2
N-benzylidene-4-iodoaniline

: 3526-49-6
N-(4-iodophenyl)benzylamine

Guidance literature:: With (4-Ph)Triaz(NHPⁱPr₂)₂Mn(CO)₂Br; potassium tert-butylate; hydrogen; In tetrahydrofuran; at 50 ℃; for 4h; under 15001.5 Torr; chemoselective reaction; Glovebox; Autoclave; Sealed tube;
DOI:10.1021/jacs.9b05024

Reference yield: 98.0%

: 52807-29-1
N-(4-iodophenyl)benzamide

: 3526-49-6
N-(4-iodophenyl)benzylamine

Guidance literature:: With 1,1,3,3-Tetramethyldisiloxane; tris(pentafluorophenyl)borate; In toluene; at 50 ℃; for 1.5h; Inert atmosphere;
DOI:10.1021/jo501299j