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2-Acetoxy-benzoic acid carbamoylmethyl ester

Base Information
  • Chemical Name:2-Acetoxy-benzoic acid carbamoylmethyl ester
  • CAS No.:50785-22-3
  • Molecular Formula:C11H11NO5
  • Molecular Weight:237.212
  • Hs Code.:
  • ChEMBL ID:CHEMBL163019
  • DSSTox Substance ID:DTXSID60876329
  • Nikkaji Number:J1.566.265D
  • Wikidata:Q82857944
2-Acetoxy-benzoic acid carbamoylmethyl ester

Synonyms:50785-22-3;2-Acetoxy-benzoic acid carbamoylmethyl ester;CHEMBL163019;SCHEMBL9651440;DTXSID60876329;BENZOIC ACID, 2-(ACETYLOXY)-, 2-AMINO-2-OXOETHYL

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-Acetoxy-benzoic acid carbamoylmethyl ester
Chemical Property:
  • XLogP3:0.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:237.06372245
  • Heavy Atom Count:17
  • Complexity:315
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=O)OC1=CC=CC=C1C(=O)OCC(=O)N
Technology Process of 2-Acetoxy-benzoic acid carbamoylmethyl ester

There total 2 articles about 2-Acetoxy-benzoic acid carbamoylmethyl ester 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:
Guidance literature:
With triethylamine; sodium iodide; In ethyl acetate; for 3h; Yield given; Heating;
DOI:10.1021/jm00123a040
Guidance literature:
Salicyloylglykolamid, Essigsaeureanhydrid;
Guidance literature:
With 10 percent human plasma; In acetonitrile; at 37 ℃; Rate constant; phosphate buffer (pH 7.4); or in undiluted plasma;
DOI:10.1021/jm00123a040
upstream raw materials:

aspirin

Chloroacetamide

Downstream raw materials:

salicyloyloxy-acetic acid amide

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