2-(Benzyloxy)acetamide

Base Information

Chemical Name:2-(Benzyloxy)acetamide
CAS No.:5774-77-6
Molecular Formula:C₉H₁₁NO₂
Molecular Weight:165.192
Hs Code.:
European Community (EC) Number:859-755-7

Synonyms:2-(benzyloxy)acetamide;5774-77-6;2-phenylmethoxyacetamide;MFCD11643255;2-benzyloxy-acetamide;benzyloxyacetamide;Phenylmethoxyacetamid;2-benzyloxyacetamide;2-(Phenylmethoxy)-acetamide;SCHEMBL203767;KPWDCOXYEPSQBD-UHFFFAOYSA-N;AKOS008021388;SB76432;BS-32583;SY176437;CS-0186437;EN300-54350;E76463;Z52214418

Suppliers and Price of 2-(Benzyloxy)acetamide

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 4 raw suppliers

Chemical Property of 2-(Benzyloxy)acetamide

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:165.078978594
Heavy Atom Count:12
Complexity:142

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)COCC(=O)N

Technology Process of 2-(Benzyloxy)acetamide

There total 5 articles about 2-(Benzyloxy)acetamide 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: 94.0%

: 32122-09-1
ethyl benzyloxyacetate

: 5774-77-6
2-(benzyloxy)acetamide

Guidance literature:: With ammonium hydroxide; In dichloromethane; at 0 ℃; for 5h;

Reference yield:

: 100-51-6,185532-71-2
benzyl alcohol

: 5774-77-6
2-(benzyloxy)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / tetrahydrofuran

2: ammonium hydroxide / dichloromethane / 5 h / 0 °C

With sodium hydride; ammonium hydroxide; In tetrahydrofuran; dichloromethane;