5-Methyl-1,2,4-thiadiazol-3-amine

Base Information

Chemical Name:5-Methyl-1,2,4-thiadiazol-3-amine
CAS No.:27182-55-4
Molecular Formula:C3H5 N3 S
Molecular Weight:115.159
Hs Code.:2934999090
European Community (EC) Number:833-090-2
DSSTox Substance ID:DTXSID70482218
Mol file:27182-55-4.mol

Synonyms:5-METHYL-1,2,4-THIADIAZOL-3-AMINE;27182-55-4;3-AMINO-5-METHYL-1,2,4-THIADIAZOLE;1,2,4-Thiadiazol-3-amine,5-methyl-;SCHEMBL367014;DTXSID70482218;XJTJCIZGMCJHTI-UHFFFAOYSA-N;MFCD11110666;AKOS006309828;AT11903;5-methyl-1, 2, 4-thiadiazol-3-amine;BS-37624;CS-0450553;EN300-82317;A818946;Z1198313987

Suppliers and Price of 5-Methyl-1,2,4-thiadiazol-3-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-methyl-1,2,4-thiadiazol-3-amine
50mg
$ 90.00

ChemBridge Corporation
5-methyl-1,2,4-thiadiazol-3-amine 95%
10 g
$ 1760.00

AK Scientific
5-Methyl-1,2,4-thiadiazol-3-amine
100mg
$ 279.00

Total 11 raw suppliers

Chemical Property of 5-Methyl-1,2,4-thiadiazol-3-amine

Chemical Property:

Melting Point:138-139 °C(Solv: benzene (71-43-2))
Boiling Point:261.2±23.0 °C(Predicted)
PKA:2.23±0.11(Predicted)
PSA：80.04000
Density:1.372±0.06 g/cm3(Predicted)
LogP:1.00990
XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:115.02041835
Heavy Atom Count:7
Complexity:67.2

Purity/Quality:

97% ^*data from raw suppliers

5-methyl-1,2,4-thiadiazol-3-amine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NC(=NS1)N

Technology Process of 5-Methyl-1,2,4-thiadiazol-3-amine

There total 2 articles about 5-Methyl-1,2,4-thiadiazol-3-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:

: 57053-68-6
N-acetylcarbamimidoyl-thioacetamide

: 27182-55-4
5-methyl-1,2,4-thiadiazol-3-amine

Guidance literature:: Multistep reaction; (i) Br₂, CHCl₃, EtOH, (ii) aq. Na₂CO₃;

Reference yield:

: 27182-55-4
5-methyl-1,2,4-thiadiazol-3-amine

Guidance literature:: Acetylguanidin, Thioessigsaeureethylester;

Reference yield: 28.0%

: 27182-55-4
5-methyl-1,2,4-thiadiazol-3-amine

: 1262849-20-6
2-bromo-4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)thiazole-5-carbonitrile

: 1355335-75-9
4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-2-(5-methyl-1,2,4-thiadiazol-3-ylamino)thiazole-5-carbonitrile

Guidance literature:: With potassium carbonate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; Inert atmosphere; Reflux;