3-Benzoylpyridine-2-carbaldehyde

Base Information

Chemical Name:3-Benzoylpyridine-2-carbaldehyde
CAS No.:167961-86-6
Molecular Formula:C13H9NO2
Molecular Weight:211.22
Hs Code.:
DSSTox Substance ID:DTXSID40569909
Nikkaji Number:J715.928E
Wikidata:Q82457170
Mol file:167961-86-6.mol

Synonyms:3-Benzoylpyridine-2-carbaldehyde;167961-86-6;SCHEMBL10119637;DTXSID40569909

Suppliers and Price of 3-Benzoylpyridine-2-carbaldehyde

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 3-Benzoylpyridine-2-carbaldehyde

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:211.063328530
Heavy Atom Count:16
Complexity:259

Purity/Quality:: 99% ^*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)C2=C(N=CC=C2)C=O

Technology Process of 3-Benzoylpyridine-2-carbaldehyde

There total 2 articles about 3-Benzoylpyridine-2-carbaldehyde 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: 60.0%

: 5220-61-1
(2-methylpyridin-3-yl)(phenyl)methanone

: 167961-86-6
3-Benzoylpyridine-2-carbaldehyde

Guidance literature:: With selenium(IV) oxide; In acetic acid; for 3h; Heating;
DOI:10.1002/ardp.19953280616

Reference yield:

: 23652-90-6
(2Z)-3-amino-1-phenylbut-2-en-1-one

: 167961-86-6
3-Benzoylpyridine-2-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 29 percent / acetic acid / 3 h / Heating

2: 60 percent / SeO₂ / acetic acid / 3 h / Heating

With selenium(IV) oxide; In acetic acid;
DOI:10.1002/ardp.19953280616