N-(oxan-2-yl)benzamide

Base Information

Chemical Name:N-(oxan-2-yl)benzamide
CAS No.:15879-41-1
Molecular Formula:C12H15NO2
Molecular Weight:205.257
Hs Code.:2932999099
European Community (EC) Number:668-496-7
DSSTox Substance ID:DTXSID40395442
Nikkaji Number:J681.478F
Mol file:15879-41-1.mol

Synonyms:N-(oxan-2-yl)benzamide;15879-41-1;N-tetrahydro-2H-pyran-2-ylbenzenecarboxamide;MS-1322;DTXSID40395442;N-tetrahydro-pyran-2-yl-benzamide;MFCD00033841;AKOS015994167;N-(TETRAHYDROPYRAN-2-YL)BENZAMIDE;N-[(Tetrahydro-2H-pyran)-2-yl]benzamide;SR-01000309859;SR-01000309859-1

Suppliers and Price of N-(oxan-2-yl)benzamide

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

Sigma-Aldrich
N-(TETRAHYDROPYRAN-2-YL)BENZAMIDE AldrichCPR
50mg
$ 144.00

American Custom Chemicals Corporation
N-TETRAHYDRO-2H-PYRAN-2-YLBENZENECARBOXAMIDE 95.00%
5MG
$ 633.99

American Custom Chemicals Corporation
N-TETRAHYDRO-2H-PYRAN-2-YLBENZENECARBOXAMIDE 95.00%
10MG
$ 631.85

American Custom Chemicals Corporation
N-TETRAHYDRO-2H-PYRAN-2-YLBENZENECARBOXAMIDE 95.00%
1MG
$ 597.89

Total 1 raw suppliers

Chemical Property of N-(oxan-2-yl)benzamide

Chemical Property:

PSA：41.82000
LogP:2.51780
XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:205.110278721
Heavy Atom Count:15
Complexity:212

Purity/Quality:

98%,99%, ^*data from raw suppliers

N-(TETRAHYDROPYRAN-2-YL)BENZAMIDE AldrichCPR ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCOC(C1)NC(=O)C2=CC=CC=C2

Technology Process of N-(oxan-2-yl)benzamide

There total 5 articles about N-(oxan-2-yl)benzamide 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: 65.0%

: 110-87-2
3,4-dihydro-2H-pyran

: 55-21-0,27208-38-4
benzamide

: 15879-41-1
N-(tetrahydro-2H-pyran-2-yl)benzamide

Guidance literature:: With toluene-4-sulfonic acid; In dichloromethane; at 20 ℃;
DOI:10.1021/ja0170448

Reference yield: 10.0%

: 694-54-2
tetrahydro-2H-2-pyranol

: 55-21-0,27208-38-4
benzamide

: 15879-41-1
N-(tetrahydro-2H-pyran-2-yl)benzamide

Guidance literature:: With rhenium(VII) oxide; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.3762/bjoc.9.174

Reference yield:

: 110-87-2
3,4-dihydro-2H-pyran

: 1310412-42-0
1-benzoylamino-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester

: 15879-41-1
N-(tetrahydro-2H-pyran-2-yl)benzamide

: 1310412-60-2,1347675-92-6,2165689-24-5
N-(tetrahydro-2H-pyran-3-yl)benzamide

Guidance literature:: With 2,2'-azobis(isobutyronitrile); thiophenol; In benzene; at 80 ℃; for 18h; regioselective reaction; Inert atmosphere;
DOI:10.1002/asia.201000881