Clobenzorex

Base Information

Chemical Name:Clobenzorex
CAS No.:76553-22-5
Molecular Formula:C₁₆H₁₈ClN
Molecular Weight:259.779
Hs Code.:
European Community (EC) Number:236-434-4,616-349-2
DSSTox Substance ID:DTXSID7048409
Nikkaji Number:J8.101I
Wikipedia:Clobenzorex
Wikidata:Q5134761
NCI Thesaurus Code:C77327
ChEMBL ID:CHEMBL1213251

Synonyms:clobenzorex;clobenzorex hydrochloride;clobenzorex, (+-)-isomer

Suppliers and Price of Clobenzorex

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 Clobenzorex

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:259.1127773
Heavy Atom Count:18
Complexity:225

Purity/Quality:: 99.9% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(CC1=CC=CC=C1)NCC2=CC=CC=C2Cl

Technology Process of Clobenzorex

There total 4 articles about Clobenzorex 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: 72.0%

: N-(2-chlorobenzyl)-4-methyl-N-(1-phenylpropan-2-yl)benzenesulfonamide

: 76553-22-5
Clobenzorex

Guidance literature:: With magnesium; In methanol; at 25 ℃;
DOI:10.1002/adsc.201600821

Reference yield:

: 6338-74-5,34542-12-6
4-methyl-N-(1-phenylpropan-2-yl)benzenesulfonamide

: 76553-22-5
Clobenzorex

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 24 h / 25 °C

2: magnesium / methanol / 25 °C

With potassium carbonate; magnesium; In methanol; acetonitrile;
DOI:10.1002/adsc.201600821

Reference yield:

: N-(1-bromo-1-phenylpropan-2-yl)-4-methylbenzenesulfonamide

: 76553-22-5
Clobenzorex

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylstannane; 2,2'-azobis(isobutyronitrile) / toluene / 110 °C

2: potassium carbonate / acetonitrile / 24 h / 25 °C

3: magnesium / methanol / 25 °C

With 2,2'-azobis(isobutyronitrile); triphenylstannane; potassium carbonate; magnesium; In methanol; toluene; acetonitrile;
DOI:10.1002/adsc.201600821