1,3,4-OXADIAZOLE, 2-AMINO-5-(m-TOLYLOXYMETHYL)-

Base Information

Chemical Name:1,3,4-OXADIAZOLE, 2-AMINO-5-(m-TOLYLOXYMETHYL)-
CAS No.:21520-92-3
Molecular Formula:C₁₀H₁₁N₃O₂
Molecular Weight:205.216
Hs Code.:
DSSTox Substance ID:DTXSID90175857
Nikkaji Number:J64.529J
Wikidata:Q83046189
Mol file:21520-92-3.mol

Synonyms:21520-92-3;5-[(3-methylphenoxy)methyl]-1,3,4-oxadiazol-2-amine;1,3,4-OXADIAZOLE, 2-AMINO-5-(m-TOLYLOXYMETHYL)-;2-Amino-5-(m-tolyloxymethyl)-1,3,4-oxadiazole;5-((3-Methylphenoxy)methyl)-1,3,4-oxadiazol-2-amine;NIOSH/RO0548500;DTXSID90175857;AOD100481;AKOS022212545;LS-99056;LS-99084;RO05485000;2-Amino-5-(m-tolyl)oxymethyl-1,3,4-oxadiazole;1,3,4-Oxadiazol-2-amine, 5-((3-methylphenoxy)methyl)-

Suppliers and Price of 1,3,4-OXADIAZOLE, 2-AMINO-5-(m-TOLYLOXYMETHYL)-

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

American Custom Chemicals Corporation
1,3,4-OXADIAZOL-2-AMINE, 5-[(3-METHYLPHENOXY)METHYL]- 95.00%
5MG
$ 497.71

Total 1 raw suppliers

Chemical Property of 1,3,4-OXADIAZOLE, 2-AMINO-5-(m-TOLYLOXYMETHYL)-

Chemical Property:

Vapor Pressure:1.27E-06mmHg at 25°C
Boiling Point:400.4°C at 760 mmHg
Flash Point:196°C
PSA：74.90000
Density:1.267g/cm³
LogP:1.46930
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:205.085126602
Heavy Atom Count:15
Complexity:203

Purity/Quality:

95% ^*data from raw suppliers

1,3,4-OXADIAZOL-2-AMINE, 5-[(3-METHYLPHENOXY)METHYL]- 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=CC=C1)OCC2=NN=C(O2)N

Technology Process of 1,3,4-OXADIAZOLE, 2-AMINO-5-(m-TOLYLOXYMETHYL)-

There total 2 articles about 1,3,4-OXADIAZOLE, 2-AMINO-5-(m-TOLYLOXYMETHYL)- 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: 99.0%

: 506-68-3
bromocyane

: 36304-38-8
m-tolyloxy-acetic acid hydrazide

: 21520-92-3
2-Amino-5-(3'-methylphenoxymethyl)-1,3,4-oxadiazole

Guidance literature:: In methanol; N,N-dimethyl-formamide; for 1h; Ambient temperature;

Reference yield:

: 63051-20-7
m-tolyloxyacetic acid methyl ester

: 21520-92-3
2-Amino-5-(3'-methylphenoxymethyl)-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / NH₂NH₂*H₂O / ethanol / 5 h / Heating

2: 99 percent / methanol; dimethylformamide / 1 h / Ambient temperature

With hydrazine hydrate; In methanol; ethanol; N,N-dimethyl-formamide;