N-{[(1,4-Dioxan-2-yl)methyl]carbamothioyl}benzamide

Base Information

Chemical Name:N-{[(1,4-Dioxan-2-yl)methyl]carbamothioyl}benzamide
CAS No.:113019-60-6
Molecular Formula:C13H16N2O3S
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID80550917

Synonyms:113019-60-6;N-{[(1,4-Dioxan-2-yl)methyl]carbamothioyl}benzamide;DTXSID80550917

Suppliers and Price of N-{[(1,4-Dioxan-2-yl)methyl]carbamothioyl}benzamide

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 1 raw suppliers

Chemical Property of N-{[(1,4-Dioxan-2-yl)methyl]carbamothioyl}benzamide

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:280.08816355
Heavy Atom Count:19
Complexity:319

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COC(CO1)CNC(=S)NC(=O)C2=CC=CC=C2

Technology Process of N-{[(1,4-Dioxan-2-yl)methyl]carbamothioyl}benzamide

There total 2 articles about N-{[(1,4-Dioxan-2-yl)methyl]carbamothioyl}benzamide 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:

: 21048-16-8
2-(chloromethyl)-1,4-dioxane

: 113019-60-6
1-(1,4-Dioxanylmethyl)-3-benzoylthiourea

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent

3: 62 percent

Reference yield:

: 113019-61-7
2-Phthalimidomethyl-1,4-dioxane

: 113019-60-6
1-(1,4-Dioxanylmethyl)-3-benzoylthiourea

Guidance literature:: Multi-step reaction with 2 steps

2: 62 percent

Reference yield:

: 113019-60-6
1-(1,4-Dioxanylmethyl)-3-benzoylthiourea

: 113019-66-2
2-[([1,4]Dioxan-2-ylmethyl)-amino]-4-phenyl-thiazole-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent

2: 45 percent / CH₃COONa / ethanol / 12 h / Heating

With sodium acetate; In ethanol;