ambuside

Base Information

Chemical Name:ambuside
CAS No.:3754-19-6
Molecular Formula:C13H16 Cl N3 O5 S2
Molecular Weight:393.872
Hs Code.:
European Community (EC) Number:223-158-4
UNII:VCM261MOO0
Nikkaji Number:J8.242B
Wikidata:Q27291757
NCI Thesaurus Code:C90837
Mol file:3754-19-6.mol

Synonyms:1,3-Benzenedisulfonamide,4-chloro-6-[(3-hydroxy-2-butenylidene)amino]-N1-2-propenyl- (9CI);m-Benzenedisulfonamide, N1-allyl-4-chloro-6-[(3-hydroxy-2-butenylidene)amino]-(7CI); m-Benzenedisulfonamide,N1-allyl-4-chloro-6-[(3-hydroxy-2-butenylidene)amino]- (8CI);2-(Allylsulfamoyl)-5-chloro-4-sulfamoyl-N-(3-hydroxy-2-butenylidene)aniline;Ambusid; Ambuside; EX 4810; Hydrion;N1-Allyl-4-chloro-6-[(3-hydroxy-2-butenylidene)amino]-m-benzenedisulfonamide;Novohydrin; RMI 83047

Suppliers and Price of ambuside

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

TRC
Ambuside
100mg
$ 1320.00

American Custom Chemicals Corporation
AMBUSIDE 95.00%
5MG
$ 496.43

Total 6 raw suppliers

Chemical Property of ambuside

Chemical Property:

Appearance/Colour:Crystals
Melting Point:205-207ºC
Boiling Point:607.4 °C at 760 mmHg
Flash Point:321.1 °C
PSA：155.68000
Density:1.465 g/cm³
LogP:4.86860
XLogP3:1.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:8
Exact Mass:393.0219907
Heavy Atom Count:24
Complexity:694

Purity/Quality:

99% ^*data from raw suppliers

Ambuside ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C=CNC1=CC(=C(C=C1S(=O)(=O)NCC=C)S(=O)(=O)N)Cl
Uses Diuretic. Ambuside is used in biological studies in the discovery of novel trypanosomicidal drug like chemicals.
Therapeutic Function Diuretic, Antihypertensive

Technology Process of ambuside

There total 1 articles about ambuside 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:

: 5436-21-5
acetylacetaldehyde dimethyl acetal

: 3921-09-3
2-Allylsulfamoyl-5-chlor-4-sulfamoyl-anilin

: 3754-19-6
ambuside

Guidance literature:: With hydrogenchloride;
DOI:10.1021/jm00325a018

Reference yield:

: 3754-19-6
ambuside

: 3921-09-3
2-Allylsulfamoyl-5-chlor-4-sulfamoyl-anilin

Guidance literature:: With sodium hydroxide;
DOI:10.1021/jm00325a018

Reference yield:

: 3754-19-6
ambuside

: 3754-21-0
N-(2-Hydroxy-3-cyclohexen-1-ylmethyliden)-2-allylsulfamoyl-5-chlor-4-sulfamoyl-anilin

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH

2: aq. HCl

With hydrogenchloride; sodium hydroxide;
DOI:10.1021/jm00325a018