4-(1H-imidazol-5-yl)-N-methylaniline

Base Information

Chemical Name:4-(1H-imidazol-5-yl)-N-methylaniline
CAS No.:89250-14-6
Molecular Formula:C10H11N3
Molecular Weight:173.217
Hs Code.:
DSSTox Substance ID:DTXSID30603487
Wikidata:Q82500909

Synonyms:89250-14-6;4-(1H-Imidazol-4-yl)-N-methylaniline;4-(1H-imidazol-5-yl)-N-methylaniline;SCHEMBL11148418;SCHEMBL21662554;DTXSID30603487;PBRXATIPHRYUEW-UHFFFAOYSA-N;AKOS012389794;N-Methyl-N-[4-(imidazol-4-yl)-phenyl]-amine

Suppliers and Price of 4-(1H-imidazol-5-yl)-N-methylaniline

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 4-(1H-imidazol-5-yl)-N-methylaniline

Chemical Property:

XLogP3:1.7
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:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC1=CC=C(C=C1)C2=CN=CN2

Technology Process of 4-(1H-imidazol-5-yl)-N-methylaniline

There total 2 articles about 4-(1H-imidazol-5-yl)-N-methylaniline 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: 66.0%

: 89250-13-5
N-(4-1H-imidazol-4-ylphenyl)formamide

: 89250-14-6
N-methyl-N-(4-1H-imidazol-4-ylphenyl)amine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 4h; Heating;

Reference yield:

: 29528-28-7
VUF 5801

: 89250-14-6
N-methyl-N-(4-1H-imidazol-4-ylphenyl)amine

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / 4 h / Heating

2: 66 percent / LiAlH₄ / tetrahydrofuran / 4 h / Heating

With lithium aluminium tetrahydride; In tetrahydrofuran;