N-(2,4,5-trimethylphenyl)acetamide

Base Information Edit

Chemical Name:N-(2,4,5-trimethylphenyl)acetamide
CAS No.:88166-77-2
Molecular Formula:C11H15NO
Molecular Weight:177.246
Hs Code.:
European Community (EC) Number:661-244-7
DSSTox Substance ID:DTXSID60399801
Wikidata:Q82202539
Mol file:88166-77-2.mol

Synonyms:N-(2,4,5-trimethylphenyl)acetamide;88166-77-2;SCHEMBL10306224;DTXSID60399801;AKOS024325180;AE-562/43458018

Suppliers and Price of N-(2,4,5-trimethylphenyl)acetamide

Supply Marketing:Edit

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 2 raw suppliers

Chemical Property of N-(2,4,5-trimethylphenyl)acetamide Edit

Chemical Property:

PSA：32.59000
LogP:3.21970
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:177.115364102
Heavy Atom Count:13
Complexity:191

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C=C1C)NC(=O)C)C

Technology Process of N-(2,4,5-trimethylphenyl)acetamide

There total 7 articles about N-(2,4,5-trimethylphenyl)acetamide 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: 90.0%

: 351002-92-1
2,4,5-trimethylphenylacetylene

: 88166-77-2
2,4,5-trimethylacetanilide

Guidance literature:: With sodium azide; C₁₆H₁₇AuBrN₃O; water; trifluoroacetic acid; In 1,2-dichloro-ethane; at 25 ℃; for 2h; regioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1016/j.jorganchem.2019.02.011