4-(1H-imidazol-4-ylmethyl)aniline

Base Information

Chemical Name:4-(1H-imidazol-4-ylmethyl)aniline
CAS No.:57662-33-6
Molecular Formula:C10H11N3
Molecular Weight:173.217
Hs Code.:
ChEMBL ID:CHEMBL506072
DSSTox Substance ID:DTXSID60481593
Wikidata:Q82317081
Mol file:57662-33-6.mol

Synonyms:57662-33-6;4-(1H-imidazol-4-ylmethyl)aniline;4-(1H-IMIDAZOL-4-YLMETHYL)-PHENYLAMINE;CHEMBL506072;SCHEMBL3149298;BDBM22547;DTXSID60481593;LKKISAMEUBGGRO-UHFFFAOYSA-N;4-(4-amino-benzyl)-1H-imidazole;4-(imidazol-4-yl-methyl)-aniline;AKOS006288766;4-[(1H-Imidazol-5-yl)methyl]aniline;4-Benzyl-1H-imidazole derivative, 25

Suppliers and Price of 4-(1H-imidazol-4-ylmethyl)aniline

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
4-(1H-IMIDAZOL-4-YLMETHYL)-PHENYLAMINE 95.00%
5MG
$ 500.70

Total 5 raw suppliers

Chemical Property of 4-(1H-imidazol-4-ylmethyl)aniline

Chemical Property:

PSA：54.70000
LogP:2.16390
XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:173.095297364
Heavy Atom Count:13
Complexity:152

Purity/Quality:

96% ^*data from raw suppliers

4-(1H-IMIDAZOL-4-YLMETHYL)-PHENYLAMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1CC2=CN=CN2)N

Technology Process of 4-(1H-imidazol-4-ylmethyl)aniline

There total 6 articles about 4-(1H-imidazol-4-ylmethyl)aniline 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: 95.0%

: 57662-32-5
4-(4-nitro-benzyl)-1H-imidazole

: 57662-33-6
VUF 5802

Guidance literature:: In EtOH on palladium; pyrographite;

Reference yield:

: 869501-14-4
acetic acid (4-nitrophenyl)-(1-trityl-1H-imidazol-4-yl)methyl ester

: 57662-33-6
VUF 5802

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 20 ℃; for 4h;
DOI:10.1016/j.bmc.2005.09.002

Reference yield:

: 555-16-8
4-nitrobenzaldehdye

: 57662-33-6
VUF 5802

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / ethylmagnesium bromide / CH₂Cl₂; tetrahydrofuran / 16 h / 20 °C

2: 95 percent / 4-(dimethylamino)pyridine / CH₂Cl₂ / 6 h / Heating

3: H₂ / Pd/C / methanol / 4 h / 20 °C

With dmap; ethylmagnesium bromide; hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.bmc.2005.09.002