1,3,5-Triazin-2-amine, N,4-dicyclopropyl-6-(4-thiomorpholinyl)-, 2,2-dioxide

Base Information

Chemical Name:1,3,5-Triazin-2-amine, N,4-dicyclopropyl-6-(4-thiomorpholinyl)-, 2,2-dioxide
CAS No.:148312-52-1
Molecular Formula:C₁₃H₁₉N₅O₂S
Molecular Weight:309.392
Hs Code.:
DSSTox Substance ID:DTXSID00163962
Nikkaji Number:J965.420H
Wikidata:Q83032967

Synonyms:1,3,5-Triazin-2-amine, N,4-dicyclopropyl-6-(4-thiomorpholinyl)-, 2,2-dioxide;N,4-Dicyclopropyl-6-(4-thiomorpholinyl)-1,3,5-triazin-2-amine 2,2-dioxide;2-Cyclopropyl-4-cyclopropylamino-6-thiomorpholino-1,3,5-triazine S,S-dioxyde;148312-52-1;SCHEMBL8320258;DTXSID00163962;LS-154947;4-[4-(Cyclopropylamino)-6-cyclopropyl-1,3,5-triazine-2-yl]thiomorpholine 1,1-dioxide

Suppliers and Price of 1,3,5-Triazin-2-amine, N,4-dicyclopropyl-6-(4-thiomorpholinyl)-, 2,2-dioxide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1,3,5-Triazin-2-amine, N,4-dicyclopropyl-6-(4-thiomorpholinyl)-, 2,2-dioxide

Chemical Property:

Vapor Pressure:1.55E-15mmHg at 25°C
Boiling Point:625°Cat760mmHg
Flash Point:331.8°C
Density:1.511g/cm³
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:309.12594604
Heavy Atom Count:21
Complexity:471

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC1C2=NC(=NC(=N2)N3CCS(=O)(=O)CC3)NC4CC4

Technology Process of 1,3,5-Triazin-2-amine, N,4-dicyclopropyl-6-(4-thiomorpholinyl)-, 2,2-dioxide

There total 1 articles about 1,3,5-Triazin-2-amine, N,4-dicyclopropyl-6-(4-thiomorpholinyl)-, 2,2-dioxide 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: 17.0%