4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline

Base Information

Chemical Name:4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline
CAS No.:10364-76-8
Molecular Formula:C₁₁H₁₃N₃O
Molecular Weight:203.244
Hs Code.:
DSSTox Substance ID:DTXSID90603802
Wikidata:Q82501341
Mol file:10364-76-8.mol

Synonyms:4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline;10364-76-8;SCHEMBL10914161;DTXSID90603802;MFCD12191345;BS-25219

Suppliers and Price of 4-(5-Propyl-1,2,4-oxadiazol-3-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

TRC
4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline
50mg
$ 90.00

Crysdot
4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline 95+%
1g
$ 330.00

AK Scientific
4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline
1g
$ 517.00

Total 5 raw suppliers

Chemical Property of 4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline

Chemical Property:

Melting Point:88 °C
Boiling Point:375.8±44.0 °C(Predicted)
PKA:1.99±0.10(Predicted)
Density:1.157±0.06 g/cm3(Predicted)
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:203.105862047
Heavy Atom Count:15
Complexity:192

Purity/Quality:

97% ^*data from raw suppliers

4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCC1=NC(=NO1)C2=CC=C(C=C2)N

Technology Process of 4-(5-Propyl-1,2,4-oxadiazol-3-yl)aniline

There total 5 articles about 4-(5-Propyl-1,2,4-oxadiazol-3-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: 54.0%

: 10364-67-7
5-propyl-3-(4-nitrophenyl)-1,2,4-oxadiazole

: 10364-76-8
3-(4'-aminophenyl)-5-propyl-1,2,4-oxadiazole

Guidance literature:: With sodium sulfide; In 1,4-dioxane; water; at 80 ℃; for 0.75h; Inert atmosphere;
DOI:10.1016/j.bmc.2014.02.013

Reference yield:

: 555-16-8
4-nitrobenzaldehdye

: 10364-76-8
3-(4'-aminophenyl)-5-propyl-1,2,4-oxadiazole

Guidance literature:: Multi-step reaction with 4 steps

1: hydroxylamine hydrochloride / dimethyl sulfoxide / 3 h / 20 - 100 °C

2: hydroxylamine hydrochloride; sodium hydroxide / water; ethanol / 36 h / Inert atmosphere; Reflux

3: pyridine / 0.5 h / Reflux; Inert atmosphere

4: sodium sulfide / 1,4-dioxane; water / 0.75 h / 80 °C / Inert atmosphere

With pyridine; sodium sulfide; hydroxylamine hydrochloride; sodium hydroxide; In 1,4-dioxane; ethanol; water; dimethyl sulfoxide;
DOI:10.1016/j.bmc.2014.02.013

Reference yield:

: 192332-48-2
(Z)-4-nitrobenzamidoxime

: 10364-76-8
3-(4'-aminophenyl)-5-propyl-1,2,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 0.5 h / Reflux; Inert atmosphere

2: sodium sulfide / 1,4-dioxane; water / 0.75 h / 80 °C / Inert atmosphere

With pyridine; sodium sulfide; In 1,4-dioxane; water;
DOI:10.1016/j.bmc.2014.02.013