N-[(Benzoyloxy)acetyl]-N-methylglycine

Base Information

Chemical Name:N-[(Benzoyloxy)acetyl]-N-methylglycine
CAS No.:106231-64-5
Molecular Formula:C12H13NO5
Molecular Weight:251.239
Hs Code.:
ChEMBL ID:CHEMBL140366
DSSTox Substance ID:DTXSID70872115
Nikkaji Number:J1.553.351J

Synonyms:N-[(Benzoyloxy)acetyl]-N-methylglycine;106231-64-5;CHEMBL140366;DTXSID70872115

Suppliers and Price of N-[(Benzoyloxy)acetyl]-N-methylglycine

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 N-[(Benzoyloxy)acetyl]-N-methylglycine

Chemical Property:

XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:251.07937252
Heavy Atom Count:18
Complexity:322

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(CC(=O)O)C(=O)COC(=O)C1=CC=CC=C1

Technology Process of N-[(Benzoyloxy)acetyl]-N-methylglycine

There total 4 articles about N-[(Benzoyloxy)acetyl]-N-methylglycine 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: 77.0%

: 107-97-1,25951-24-0
sarcosine

: 54150-57-1
2-benzoyloxyacetyl chloride

: 106231-64-5
2-(benzoyloxy)-(N-methyl-N-acetic acid)acetamide

Guidance literature:: With sodium hydroxide; In benzene; for 1h; Ambient temperature;
DOI:10.1002/jps.2600770402

Reference yield:

: 532-32-1
sodium benzoate

: 106231-64-5
2-(benzoyloxy)-(N-methyl-N-acetic acid)acetamide

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: 77 percent / aq. NaOH / benzene / 1 h / 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

: 106231-64-5
2-(benzoyloxy)-(N-methyl-N-acetic acid)acetamide

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: 77 percent / aq. NaOH / benzene / 1 h / Ambient temperature

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