N-(3,5-dimethylphenyl)-4-methoxybenzamide

Base Information

Chemical Name:N-(3,5-dimethylphenyl)-4-methoxybenzamide
CAS No.:127291-98-9
Molecular Formula:C₁₆H₁₇NO₂
Molecular Weight:255.316
Hs Code.:
DSSTox Substance ID:DTXSID801269788
Nikkaji Number:J3.505.529K
ChEMBL ID:CHEMBL1214631

Synonyms:N-(3,5-dimethylphenyl)-4-methoxybenzamide;127291-98-9;starbld0006210;Cambridge id 5350132;Oprea1_711306;Oprea1_728796;CHEMBL1214631;DTXSID801269788;MFCD00783882;STK026890;AKOS001214475;4-Methoxy-N-(3,5-dimethylphenyl)benzamide;J3.505.529K;N~1~-(3,5-dimethylphenyl)-4-methoxybenzamide;AB00082149-01;AK-968/11164934;Z30889723

Suppliers and Price of N-(3,5-dimethylphenyl)-4-methoxybenzamide

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
N-(3,5-DIMETHYLPHENYL)-4-METHOXYBENZAMIDE 95.00%
5MG
$ 504.49

Total 3 raw suppliers

Chemical Property of N-(3,5-dimethylphenyl)-4-methoxybenzamide

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:255.125928785
Heavy Atom Count:19
Complexity:287

Purity/Quality:

98% ^*data from raw suppliers

N-(3,5-DIMETHYLPHENYL)-4-METHOXYBENZAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=CC(=C1)NC(=O)C2=CC=C(C=C2)OC)C

Technology Process of N-(3,5-dimethylphenyl)-4-methoxybenzamide

There total 5 articles about N-(3,5-dimethylphenyl)-4-methoxybenzamide 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: 81.0%

: 203321-89-5
(3,5-dimethylphenyl)carbamic acid 1,1-dimethylethyl ester

: 7294-51-1
2,4,6-tris(4-methoxyphenyl)boroxine

: 127291-98-9
N-(3,5-dimethylphenyl)-4-methoxybenzamide

Guidance literature:: With potassium fluoride; chloro(1,5-cyclooctadiene)rhodium(I) dimer; In 1,4-dioxane; at 100 ℃; for 16h; Inert atmosphere; Sealed tube;
DOI:10.1021/acs.orglett.5b03061

Reference yield: 70.0%

: 155826-85-0
4-methoxylphenylboronic acid 1,3-propanediol ester

: 54132-75-1
3,5-dimethylphenyl isocyanate

: 127291-98-9
N-(3,5-dimethylphenyl)-4-methoxybenzamide

Guidance literature:: With copper(l) iodide; lithium tert-butoxide; In N,N-dimethyl-formamide; at 140 ℃; for 16h; Inert atmosphere;
DOI:10.1039/c5gc01374g

Reference yield:

: 54132-75-1
3,5-dimethylphenyl isocyanate

: 127291-98-9
N-(3,5-dimethylphenyl)-4-methoxybenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 16 h / 80 °C / Inert atmosphere

2: chloro(1,5-cyclooctadiene)rhodium(I) dimer; potassium fluoride / 1,4-dioxane / 16 h / 100 °C / Inert atmosphere; Sealed tube

With potassium fluoride; chloro(1,5-cyclooctadiene)rhodium(I) dimer; In 1,4-dioxane;
DOI:10.1021/acs.orglett.5b03061