N-Formyl-2-hydroxybenzamide

Base Information

Chemical Name:N-Formyl-2-hydroxybenzamide
CAS No.:67936-24-7
Molecular Formula:C8H7NO3
Molecular Weight:165.148
Hs Code.:
DSSTox Substance ID:DTXSID30511891
Nikkaji Number:J429.075E
Wikidata:Q82370905

Synonyms:N-Formyl-2-hydroxybenzamide;67936-24-7;N-formylsalicylamide;SCHEMBL2132346;DTXSID30511891;MFCD10568307;AKOS006303602;AS-5436;CS-0331387

Suppliers and Price of N-Formyl-2-hydroxybenzamide

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 N-Formyl-2-hydroxybenzamide

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:165.042593085
Heavy Atom Count:12
Complexity:181

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)NC=O)O

Technology Process of N-Formyl-2-hydroxybenzamide

There total 5 articles about N-Formyl-2-hydroxybenzamide 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: 75.0%

: N¹,N¹-dimethyl-N²-salicyloylformamidine

: 67936-24-7
N-formyl-2-hydroxybenzamide

Guidance literature:: With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; In ethyl acetate; at 0 - 80 ℃; for 12h; Inert atmosphere;
DOI:10.1016/j.tetlet.2015.12.046

Reference yield:

: 65-45-2
salicylamide

: 67936-24-7
N-formyl-2-hydroxybenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 53 percent / pyridine / CHCl₃ / 1 h / 0 °C

2: pyridine / toluene / Heating

With pyridine; In chloroform; toluene;