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guanoxabenz

CAS No.
24047-25-4
Chemical Name:
guanoxabenz
Synonyms
43-663;guanoxabenz;Hydroxyguanabenz;1-[(2,6-Dichlorobenzylidene)amino]-3-hydroxyguanidine;Hydrazinecarboximidamide, 2-[(2,6-dichlorophenyl)methylene]-N-hydroxy-
CBNumber:
CB41368413
Molecular Formula:
C8H8Cl2N4O
Molecular Weight:
247.084
MDL Number:
MFCD00871675
MOL File:
24047-25-4.mol
MSDS File:
SDS
Last updated:2023-05-21 10:59:17

guanoxabenz Properties

Boiling point 383.1±52.0 °C(Predicted)
Density 1.54±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka 12.30±0.70(Predicted)
FDA UNII P9HIK5V7WK
ATC code C02CC07

guanoxabenz price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0011595 GUANOXABENZ 95.00% 24047-25-4 5MG $497.65 2021-12-16 Buy
Product number Packaging Price Buy
API0011595 5MG $497.65 Buy

guanoxabenz Chemical Properties,Uses,Production

Originator

Benezrial,Houde,France,1978

Uses

Antihypertensive.

Definition

ChEBI: Guanoxabenz is a dichlorobenzene.

Manufacturing Process

2N sodium hydroxide solution (5 ml) is added to a stirred suspension of Smethylisothiosemicarbazide hydroiodide (2.33 g) and hydroxylamine hydrochloride (0.70 g) in water (6 ml) and stirred for 48 hours. The solution is evaporated in vacuo to provide 1-amino-3-hydroxyguanidine. One-third of the residue is dissolved in 16 ml of ethanol and 2,6-dichlorobenzaldehyde (0.6 g) is added to this solution. The reaction mixture is then stirred for 48 hours. The solution is then evaporated in vacuo and the residue dissolved in ether (30 ml) and in hydrochloric acid (30 ml). The aqueous phase is rendered alkaline with 2N sodium carbonate solution and extracted with ether. The ether layer is dried with sodium sulfate and evaporated. The residue is dissolved in ether and excess dry hydrogen chloride is passed into the solution.
The resultant mixture is evaporated in vacuo and the residue triturated with methylene chloride to afford a crude product. Recrystallization from ethanolether (1:3) provides 1-(2,6-dichlorobenzylideneamino)-3-hydroxyguanidine hydrochloride; MP 173°C to 175°C. When the above process is carried out and S-benzylisothiosemicarbazide hydroiodide is used in place of S-methylisothiosemicarbazide hydroiodide, the identical product is again obtained.

Therapeutic Function

Antihypertensive

guanoxabenz Preparation Products And Raw materials

guanoxabenz Suppliers

Global( 9)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
MedChemexpress LLC 021-58955995 sales@medchemexpress.cn United States 4863 58
Fan De(Beijing) Biotechnology Co., Ltd. 15911056312 liming@bio-fount.com China 9730 58
BOC Sciences -- info@bocsci.com USA 0 65
Beijing Jin Ming Biotechnology Co., Ltd. 010-60605840 15801484223; psaitong@jm-bio.com China 29778 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 21667 58

24047-25-4(guanoxabenz)Related Search:

guanoxabenz 1-[(2,6-Dichlorobenzylidene)amino]-3-hydroxyguanidine 43-663 Hydroxyguanabenz Hydrazinecarboximidamide, 2-[(2,6-dichlorophenyl)methylene]-N-hydroxy- 24047-25-4