4-Acetamido-2-methylphenyl acetate

Base Information

Chemical Name:4-Acetamido-2-methylphenyl acetate
CAS No.:46420-19-3
Molecular Formula:C11H13NO3
Molecular Weight:207.229
Hs Code.:
DSSTox Substance ID:DTXSID70693504
Wikidata:Q82622551
Mol file:46420-19-3.mol

Synonyms:4-Acetamido-2-methylphenyl acetate;46420-19-3;SCHEMBL5735290;DTXSID70693504;CJWGHQUZDOJSMR-UHFFFAOYSA-N;4-(acetylamino)-2-methylphenyl acetate

Suppliers and Price of 4-Acetamido-2-methylphenyl acetate

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-Acetamido-2-methylphenyl acetate

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:207.08954328
Heavy Atom Count:15
Complexity:252

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 4-Acetamido-2-methylphenyl acetate

There total 4 articles about 4-Acetamido-2-methylphenyl acetate 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: 92.0%

: 2835-96-3
4-amino-2-methylphenol

: 108-24-7
acetic anhydride

: 46420-19-3
4'-acetoxy-3'-methylacetanilide

Guidance literature:: at 80 ℃; for 2h;

Reference yield: 73.0%

: 537-92-8
3-Methylacetanilide

: 64-19-7,77671-22-8
acetic acid

: 46420-19-3
4'-acetoxy-3'-methylacetanilide

Guidance literature:: With boron trifluoride diethyl etherate; bis-[(trifluoroacetoxy)iodo]benzene; at 20 ℃; for 0.5h; regioselective reaction;
DOI:10.1039/c0ob00749h