5-Butyl-1,3,4-oxadiazol-2-amine

Base Information

Chemical Name:5-Butyl-1,3,4-oxadiazol-2-amine
CAS No.:52838-38-7
Molecular Formula:C6H11N3O
Molecular Weight:141.17
Hs Code.:2934999090
European Community (EC) Number:894-460-7
DSSTox Substance ID:DTXSID20511880
Nikkaji Number:J1.570.785B
Wikidata:Q82370891
Mol file:52838-38-7.mol

Synonyms:5-butyl-1,3,4-oxadiazol-2-amine;52838-38-7;5-BUTYL-1,3,4-OXADIAZOL-2-YLAMINE;DTXSID20511880;2-N-MORPHOLINOETHYLACRYLATE;2-amino-5-butyl-1,3,4-oxadiazole;AKOS000152642;FT-0620185;EN300-42438;Z285233900

Suppliers and Price of 5-Butyl-1,3,4-oxadiazol-2-amine

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
5-butyl-1,3,4-oxadiazol-2-amine
500mg
$ 310.00

American Custom Chemicals Corporation
5-BUTYL-1,3,4-OXADIAZOL-2-AMINE 95.00%
5G
$ 1168.42

American Custom Chemicals Corporation
5-BUTYL-1,3,4-OXADIAZOL-2-AMINE 95.00%
2.5G
$ 983.88

American Custom Chemicals Corporation
5-BUTYL-1,3,4-OXADIAZOL-2-AMINE 95.00%
1G
$ 721.57

AK Scientific
5-Butyl-1,3,4-oxadiazol-2-amine
2.5g
$ 664.00

AK Scientific
5-Butyl-1,3,4-oxadiazol-2-amine
1g
$ 387.00

Total 2 raw suppliers

Chemical Property of 5-Butyl-1,3,4-oxadiazol-2-amine

Chemical Property:

Vapor Pressure:0.013mmHg at 25°C
Boiling Point:259.752°C at 760 mmHg
Flash Point:110.895°C
PSA：65.67000
Density:1.113g/cm³
LogP:0.92450
XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:141.090211983
Heavy Atom Count:10
Complexity:99

Purity/Quality:: 5-butyl-1,3,4-oxadiazol-2-amine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC1=NN=C(O1)N

Technology Process of 5-Butyl-1,3,4-oxadiazol-2-amine

There total 1 articles about 5-Butyl-1,3,4-oxadiazol-2-amine 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:

: 52838-38-7
5-butyl-[1,3,4]oxadiazol-2-ylamine

Guidance literature:: Valerylhydrazid, Bromcyan;

Reference yield: 25.0%

: 4998-07-6
4,5-dimethoxy-2-nitro-benzoic acid

: 52838-38-7
5-butyl-[1,3,4]oxadiazol-2-ylamine

: N-(5-butyl-1,3,4-oxadiazol-2-yl)-4,5-dimethoxy-2-nitrobenzamide

Guidance literature:: 4,5-dimethoxy-2-nitro-benzoic acid; With N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide;

5-butyl-[1,3,4]oxadiazol-2-ylamine; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.chembiol.2017.12.011