5H-1,3,4-Thiadiazolo(2,3-b)quinazolin-5-one, 6,7,8,9-tetrahydro-2-ethyl-

Base Information

Chemical Name:5H-1,3,4-Thiadiazolo(2,3-b)quinazolin-5-one, 6,7,8,9-tetrahydro-2-ethyl-
CAS No.:116805-49-3
Molecular Formula:C₁₁H₁₃N₃OS
Molecular Weight:235.31
Hs Code.:
DSSTox Substance ID:DTXSID80151524
Nikkaji Number:J625.720H
Wikidata:Q83017988
Mol file:116805-49-3.mol

Synonyms:BRN 5030543;5H-1,3,4-Thiadiazolo(2,3-b)quinazolin-5-one, 6,7,8,9-tetrahydro-2-ethyl-;6,7,8,9-Tetrahydro-2-ethyl-5H-1,3,4-thiadiazolo(2,3-b)quinazolin-5-one;116805-49-3;DTXSID80151524;LS-150367;2-Ethyl-6,7,8,9-tetrahydro-5H-1,3,4-thiadiazolo[2,3-b]quinazolin-5-one

Suppliers and Price of 5H-1,3,4-Thiadiazolo(2,3-b)quinazolin-5-one, 6,7,8,9-tetrahydro-2-ethyl-

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

Total 0 raw suppliers

Chemical Property of 5H-1,3,4-Thiadiazolo(2,3-b)quinazolin-5-one, 6,7,8,9-tetrahydro-2-ethyl-

Chemical Property:

Vapor Pressure:9.62E-06mmHg at 25°C
Boiling Point:372.4°C at 760 mmHg
Flash Point:179°C
Density:1.51g/cm³
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:235.07793322
Heavy Atom Count:16
Complexity:450

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=NN2C(=O)C3=C(CCCC3)N=C2S1

Technology Process of 5H-1,3,4-Thiadiazolo(2,3-b)quinazolin-5-one, 6,7,8,9-tetrahydro-2-ethyl-

There total 2 articles about 5H-1,3,4-Thiadiazolo(2,3-b)quinazolin-5-one, 6,7,8,9-tetrahydro-2-ethyl- 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: 20.0%