Benzoic acid methylcarbamoylmethyl ester

Base Information

Chemical Name:Benzoic acid methylcarbamoylmethyl ester
CAS No.:106231-50-9
Molecular Formula:C10H11NO3
Molecular Weight:193.202
Hs Code.:
ChEMBL ID:CHEMBL138928
DSSTox Substance ID:DTXSID10554746
Nikkaji Number:J1.552.856G
Wikidata:Q82435902

Synonyms:106231-50-9;Benzoic acid methylcarbamoylmethyl ester;CHEMBL138928;DTXSID10554746;2-(Methylamino)-2-oxoethyl benzoate

Suppliers and Price of Benzoic acid methylcarbamoylmethyl ester

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

Total 1 raw suppliers

Chemical Property of Benzoic acid methylcarbamoylmethyl ester

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:193.07389321
Heavy Atom Count:14
Complexity:209

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC(=O)COC(=O)C1=CC=CC=C1

Technology Process of Benzoic acid methylcarbamoylmethyl ester

There total 6 articles about Benzoic acid methylcarbamoylmethyl 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:

Reference yield:

: 614-44-8
benzoyloxyacetic acid

: 106231-50-9
2-(benzoyloxy)-N-methylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / SOCl₂ / 3 h / Heating

2: aq. NaOH / benzene / Ambient temperature

With sodium hydroxide; thionyl chloride; In benzene;
DOI:10.1002/jps.2600770402

Reference yield:

: 532-32-1
sodium benzoate

: 106231-50-9
2-(benzoyloxy)-N-methylacetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / NaI / H₂O / 6 h / 90 °C

2: 80 percent / aq. HCl / 0.17 h / 75 °C

3: 88 percent / SOCl₂ / 3 h / Heating

4: aq. NaOH / benzene / Ambient temperature

With hydrogenchloride; sodium hydroxide; thionyl chloride; sodium iodide; In water; benzene;
DOI:10.1002/jps.2600770402

Reference yield:

: 64649-43-0
(aminocarbonyl)methyl benzoate

: 106231-50-9
2-(benzoyloxy)-N-methylacetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / aq. HCl / 0.17 h / 75 °C

2: 88 percent / SOCl₂ / 3 h / Heating

3: aq. NaOH / benzene / Ambient temperature

With hydrogenchloride; sodium hydroxide; thionyl chloride; In benzene;
DOI:10.1002/jps.2600770402