4-[(3-bromo-4-methoxyphenyl)sulfonylamino]-N-phenylbenzamide

Base Information

Chemical Name:4-[(3-bromo-4-methoxyphenyl)sulfonylamino]-N-phenylbenzamide
CAS No.:6158-95-8
Molecular Formula:C₁₁H₁₀Cl₂N₂O₅
Molecular Weight:321.117
Hs Code.:
DSSTox Substance ID:DTXSID70360582
Wikidata:Q82142393

Synonyms:6158-95-8;4-[(3-bromo-4-methoxyphenyl)sulfonylamino]-N-phenylbenzamide;CBMicro_002115;DTXSID70360582;SMSF0015794;STL416872;AKOS000383552;CB03613;CCG-328718;BIM-0002126.P001;4-{[(3-bromo-4-methoxyphenyl)sulfonyl]amino}-N-phenylbenzamide

Suppliers and Price of 4-[(3-bromo-4-methoxyphenyl)sulfonylamino]-N-phenylbenzamide

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 4-[(3-bromo-4-methoxyphenyl)sulfonylamino]-N-phenylbenzamide

Chemical Property:

Vapor Pressure:1.96E-14mmHg at 25°C
Boiling Point:583°Cat760mmHg
Flash Point:306.4°C
Density:1.534g/cm³
XLogP3:3.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:460.00924
Heavy Atom Count:28
Complexity:610

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)S(=O)(=O)NC2=CC=C(C=C2)C(=O)NC3=CC=CC=C3)Br

Technology Process of 4-[(3-bromo-4-methoxyphenyl)sulfonylamino]-N-phenylbenzamide

There total 4 articles about 4-[(3-bromo-4-methoxyphenyl)sulfonylamino]-N-phenylbenzamide 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:

: 134-90-7,85666-84-8
L-threo-chloramphenicol

: 6158-95-8,26367-75-9,61849-50-1
(S)-2-(2,2-dichloro-acetylamino)-3-hydroxy-1-(4-nitro-phenyl)-propan-1-one

Guidance literature:: With potassium permanganate; sulfuric acid; acetic acid;

Reference yield:

: 119-62-0,716-61-0,2792-51-0,2792-52-1,2964-48-9,3689-55-2,63526-31-8,71115-69-0,140694-64-0
(1S,2S)-2-amino-1-(4-nitrophenyl)propane-1,3-diol

: 6158-95-8,26367-75-9,61849-50-1
(S)-2-(2,2-dichloro-acetylamino)-3-hydroxy-1-(4-nitro-phenyl)-propan-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: isoamyl alcohol

2: CrO₃

With chromium(VI) oxide; i-Amyl alcohol;

Reference yield:

: 119-62-0,716-61-0,2792-51-0,2792-52-1,2964-48-9,3689-55-2,63526-31-8,71115-69-0,140694-64-0
(+/-)-threo-1-(4-nitro-phenyl)-2-amino-1,3-propanediol

: 6158-95-8,26367-75-9,61849-50-1
(S)-2-(2,2-dichloro-acetylamino)-3-hydroxy-1-(4-nitro-phenyl)-propan-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: L_g-tartaric acid

2: isoamyl alcohol

3: CrO₃

With chromium(VI) oxide; i-Amyl alcohol; L-Tartaric acid;