N-Phenyl-N'-propan-2-ylsulfuric diamide

Base Information

Chemical Name:N-Phenyl-N'-propan-2-ylsulfuric diamide
CAS No.:69705-83-5
Molecular Formula:C9H14N2O2S
Molecular Weight:214.288
Hs Code.:
DSSTox Substance ID:DTXSID30500644
Wikidata:Q82352417

Synonyms:N-Phenyl-N'-propan-2-ylsulfuric diamide;69705-83-5;SCHEMBL8312186;DTXSID30500644

Suppliers and Price of N-Phenyl-N'-propan-2-ylsulfuric diamide

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-Phenyl-N'-propan-2-ylsulfuric diamide

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:214.07759887
Heavy Atom Count:14
Complexity:251

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)NS(=O)(=O)NC1=CC=CC=C1

Technology Process of N-Phenyl-N'-propan-2-ylsulfuric diamide

There total 3 articles about N-Phenyl-N'-propan-2-ylsulfuric diamide 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: 87.0%

: 87708-16-5
N-phenyl-2-oxooxazolidine-3-sulfonamide

: 75-31-0
isopropylamine

: 69705-83-5
N-isopropyl-N'-phenyl-sulfamide

Guidance literature:: In acetonitrile; at 20 - 40 ℃; for 2h;
DOI:10.1021/op0600106

Reference yield: 80.0%

: C₉H₁₃IN₂O₂S

: 69705-83-5
N-isopropyl-N'-phenyl-sulfamide

Guidance literature:: C₉H₁₃IN₂O₂S; With methylmagnesium bromide; In tetrahydrofuran; at 0 ℃; for 1h;

With tert.-butyl lithium; In tetrahydrofuran; at -78 ℃; for 0.5h;

With cyclopentanone; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1016/S0040-4039(00)01778-0