N-[2-(1,3-benzoxazol-2-yl)phenyl]-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-[2-(1,3-benzoxazol-2-yl)phenyl]-4-methylbenzenesulfonamide
CAS No.:42143-49-7
Molecular Formula:C20H16N2O3S
Molecular Weight:364.425
Hs Code.:
DSSTox Substance ID:DTXSID701205820
Nikkaji Number:J2.425.500J
Wikidata:Q27145245
ChEMBL ID:CHEMBL2447933
Mol file:42143-49-7.mol

Synonyms:N-[2-(1,3-benzoxazol-2-yl)phenyl]-4-methylbenzenesulfonamide;CHEBI:75359;CBChromo1_000126;Probes1_000172;Probes2_000345;Oprea1_362513;CBDivE_010067;SCHEMBL6862724;CHEMBL2447933;DTXSID701205820;2-(2'-tosylaminophenyl)benzoxazole;STL181379;AKOS005373840;2-(2-(p-toluenesulfonylamino)phenyl)benzoxazole;N-(2-benzooxazol-2-yl-phenyl)-toluene-4-sulfonamide;N-[2-(Benzoxazole-2-yl)phenyl]-p-toluenesulfonamide;Q27145245;N-[2-(2-Benzoxazolyl)phenyl]-4-methylbenzenesulfonamide;42143-49-7

Suppliers and Price of N-[2-(1,3-benzoxazol-2-yl)phenyl]-4-methylbenzenesulfonamide

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 0 raw suppliers

Chemical Property of N-[2-(1,3-benzoxazol-2-yl)phenyl]-4-methylbenzenesulfonamide

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:364.08816355
Heavy Atom Count:26
Complexity:568

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)NC2=CC=CC=C2C3=NC4=CC=CC=C4O3

Technology Process of N-[2-(1,3-benzoxazol-2-yl)phenyl]-4-methylbenzenesulfonamide

There total 4 articles about N-[2-(1,3-benzoxazol-2-yl)phenyl]-4-methylbenzenesulfonamide 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: 95.0%

: 98-59-9
p-toluenesulfonyl chloride

: 29483-74-7
2-(2-aminophenyl)benzoxazole

: 42143-49-7
N-(2-(benzo[d]oxazol-2-yl)phenyl)-4-methylbenzenesulfonamide

Guidance literature:: With pyridine; at 20 ℃; for 10h;
DOI:10.1021/jo061634c

Reference yield: 88.0%

: 941-55-9
4-toluenesulfonyl azide

: 833-50-1
2-phenylbenzo[d]oxazole

: 42143-49-7
N-(2-(benzo[d]oxazol-2-yl)phenyl)-4-methylbenzenesulfonamide

Guidance literature:: With RuHCl(CO)(PPh₃)₃; In 1,2-dichloro-ethane; at 100 ℃; for 12h; Sealed tube; Inert atmosphere;
DOI:10.1021/acs.joc.8b02123