Acetamide, N-[(2-methylphenyl)methyl]-

Base Information

Chemical Name:Acetamide, N-[(2-methylphenyl)methyl]-
CAS No.:91817-68-4
Molecular Formula:C10H13NO
Molecular Weight:163.219
Hs Code.:
Mol file:91817-68-4.mol

Synonyms:Acetamide, N-(o-methylbenzyl)-;ACETAMIDE, N-[(2-METHYLPHENYL)METHYL]-;N-(2-Methylbenzyl)acetamide;

Suppliers and Price of Acetamide, N-[(2-methylphenyl)methyl]-

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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price

Total 6 raw suppliers

Chemical Property of Acetamide, N-[(2-methylphenyl)methyl]-

Chemical Property:

Melting Point:87-89 °C
Boiling Point:350.1±21.0 °C (760 mmHg)
PSA：29.10000
Density:1.013±0.06 g/cm3 (20 °C, 760 mmHg)
LogP:2.02200

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

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Technology Process of Acetamide, N-[(2-methylphenyl)methyl]-

There total 12 articles about Acetamide, N-[(2-methylphenyl)methyl]- 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: 98.0%

: 552-45-4
1-chloromethyl-2-methylbenzene

: 75-05-8,26809-02-9
acetonitrile

: 91817-68-4
N-[(2-methylphenyl)methyl]acetamide

Guidance literature:: With iron(III) chloride; for 6h; Heating;
DOI:10.1080/00397919308018613

Reference yield: 86.0%

: 89-95-2
2-methyl-benzyl alcohol

: 75-05-8,26809-02-9
acetonitrile

: 91817-68-4
N-[(2-methylphenyl)methyl]acetamide

Guidance literature:: With SiO₂ coated on magnetic CoFe₂O₄ nanoparticle immobilized N-propyldiethylenetriamine sulfamic acid; at 80 ℃; for 4h; Green chemistry;
DOI:10.1016/j.apcata.2014.06.006