N-(2-Hydroxybenzyl)acetamide

Base Information

Chemical Name:N-(2-Hydroxybenzyl)acetamide
CAS No.:80311-94-0
Molecular Formula:C9H11NO2
Molecular Weight:165.192
Hs Code.:
DSSTox Substance ID:DTXSID40507760

Synonyms:N-(2-Hydroxybenzyl)acetamide;80311-94-0;N-[(2-Hydroxyphenyl)methyl]acetamide;Acetamide, N-[(2-hydroxyphenyl)methyl]-;N-Salicylacetamid;SCHEMBL4362706;DTXSID40507760;CLTHXCBZMXABDP-UHFFFAOYSA-N;MFCD24392089;AKOS022636982;SB76226;DS-19671;CS-0160433;C76570;A922642

Suppliers and Price of N-(2-Hydroxybenzyl)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 6 raw suppliers

Chemical Property of N-(2-Hydroxybenzyl)acetamide

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:165.078978594
Heavy Atom Count:12
Complexity:159

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NCC1=CC=CC=C1O

Technology Process of N-(2-Hydroxybenzyl)acetamide

There total 15 articles about N-(2-Hydroxybenzyl)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: 71.7%

: 63452-53-9
N-acetyl-2-methoxybenzylamine

: 80311-94-0
N-(2-hydroxybenzyl)acetamide

Guidance literature:: With boron tribromide; In dichloromethane; at -10 - 20 ℃; for 2h; Inert atmosphere;

Reference yield: 65.0%

: C₁₅H₂₄N₄O

: 80311-94-0
N-(2-hydroxybenzyl)acetamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane;
DOI:10.1016/j.tetlet.2009.02.184

Reference yield: 12.0%

: 588-46-5
N-(phenylmethyl)acetamide

: 34185-04-1
N-(4-hydroxybenzyl)acetamide

: 80311-94-0
N-(2-hydroxybenzyl)acetamide

Guidance literature:: With potassium superoxide; 18-crown-6 ether; In benzene; for 168h; Mechanism; Product distribution; Ambient temperature; aromatic ortho and para hydroxylation of various N-benzylamides with potassium superoxide;
DOI:10.1016/S0040-4020(01)97990-6