2-[5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl]aniline

Base Information

Chemical Name:2-[5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl]aniline
CAS No.:120107-40-6
Molecular Formula:C₁₄H₁₀ClN₃O
Molecular Weight:271.706
Hs Code.:2934999090
DSSTox Substance ID:DTXSID50400814
Nikkaji Number:J3.414.814G
ChEMBL ID:CHEMBL2236016
Mol file:120107-40-6.mol

Synonyms:120107-40-6;2-[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]aniline;2-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)aniline;2-(2-AMINOPHENYL)-5-(4-CHLOROPHENYL)-1,3,4-OXADIAZOLE;DISPERSEYELLOW64;CHEMBL2236016;DTXSID50400814;STL300307;AKOS016051997;AO-365/43474001;2-[5-(4-Chlorophenyl)-1,3,4-oxadiazole-2-yl]aniline;2-[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]phenylamine

Suppliers and Price of 2-[5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl]aniline

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

Crysdot
2-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)aniline 95+%
5g
$ 1538.00

Crysdot
2-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)aniline 95+%
1g
$ 545.00

Total 2 raw suppliers

Chemical Property of 2-[5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl]aniline

Chemical Property:

PSA：64.94000
LogP:4.22040
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:271.0512396
Heavy Atom Count:19
Complexity:296

Purity/Quality:

97% ^*data from raw suppliers

2-(5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl)aniline 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C2=NN=C(O2)C3=CC=C(C=C3)Cl)N

Technology Process of 2-[5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl]aniline

There total 3 articles about 2-[5-(4-Chlorophenyl)-1,3,4-oxadiazol-2-yl]aniline 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: 80.3%

: 1904-58-1
anthranilic acid hydrazide

: 74-11-3
para-chlorobenzoic acid

: 120107-40-6
2-[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]-benzenamine

Guidance literature:: With trichlorophosphate; for 3h; Reflux;
DOI:10.1007/s00044-010-9480-5

Reference yield: 39.0%

: 1904-58-1
anthranilic acid hydrazide

: 74-11-3
para-chlorobenzoic acid

: 28864-30-4
N'-[(2-aminophenyl)carbonyl]-4-chlorobenzoylhydrazide

: 120107-40-6
2-[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]-benzenamine

: 104655-42-7
2-(4-chlorophenyl)-3,4-dihydro-5H-1,3,4-benzotriazepin-5-one

Guidance literature:: at 230 ℃; for 6h;

Reference yield:

: 134-20-3
2-carbomethoxyaniline

: 120107-40-6
2-[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]-benzenamine

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / ethanol / 5 h / Reflux

2: trichlorophosphate / 3 h / Reflux

With hydrazine hydrate; trichlorophosphate; In ethanol;
DOI:10.1007/s00044-010-9480-5