CAS 106649-95-0

N-Sulphamyl-3-chloropropionamidine hydrochloride

Description:

N-Sulphamyl-3-chloropropionamidine hydrochloride is a chemical compound characterized by its sulfonamide structure, which typically imparts antibacterial properties. This substance features a chloropropionamidine moiety, contributing to its potential biological activity. It is a white to off-white crystalline powder, soluble in water, which is a common trait for many sulfonamide derivatives. The hydrochloride form indicates that it is a salt, enhancing its stability and solubility in aqueous solutions. This compound may exhibit a range of pharmacological effects, particularly in the field of medicinal chemistry, where it could be investigated for its efficacy against various pathogens. Its specific interactions and mechanisms of action would depend on its molecular structure and the presence of functional groups that facilitate binding to biological targets. As with many chemical substances, safety data and handling precautions are essential, as sulfonamides can cause allergic reactions in some individuals. Overall, N-Sulphamyl-3-chloropropionamidine hydrochloride represents a compound of interest in both research and potential therapeutic applications.

Formula: C₃H₉Cl₂N₃O₂S

InChI: InChI=1/C3H8ClN3O2S.ClH/c4-2-1-3(5)7-10(6,8)9;/h1-2H2,(H2,5,7)(H2,6,8,9);1H

InChI key: InChIKey=IVLQMIVEODCGLH-UHFFFAOYSA-N

SMILES: C(NS(N)(=O)=O)(CCCl)=N.Cl

Synonyms:

• (1E)-3-chloro-N'-sulfamoylpropanimidamide hydrochloride (1:1)
• N-(Amino Sulfonyl)-3-Chloro Propanimidamide
• N-Sulfamoyl-3-chloropropionamidine
• N-Sulfamyl-3-chloromethylthiazole hydrochloride
• N-Sulfamyl-3-chloropropionamidenehydrochloride
• N-Sulfamyl-3-chloropropionamidine hydrochloride
• N-Sulphamyl-3-Chloropropionamidime
• N-Sulphamyl-3-chloropropionamidine HCL
• Propanimidamide, N-(aminosulfonyl)-3-chloro-, hydrochloride (1:1)
• Propanimidamide, N-(aminosulfonyl)-3-chloro-, monohydrochloride
• N-(Aminesulphonyl)-3-chloropropionamidine hydrochloride
• SUF (S) DE COMPRA
• N-sulphamyl-3-chloropropionamidine RS
• 3-Chloro-N-sulfamoylpropanimidamide HCl
• Famotidine side chain
• N-Sulphamyl-3-chloropropionamidine hydrochloride
• Famotidine Impurity 23
• N-Sulphamyl-3-chloropropionamidine hydrochlorid
• 3-Chloro-N-sulfamoylpropanimidamidehydrochloride

N-Sulphamyl-3-chloropropionamidine hydrochloride

CAS: 106649-95-0

Formula: C₃H₉Cl₂N₃O₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 222.0935

Ref: IN-DA008R0T

3-Chloro-N-sulfamoylpropanimidamide hydrochloride

CAS: 106649-95-0

3-Chloro-N-sulfamoylpropanimidamide hydrochloride

Purity: 95%

Ref: 54-OR1037090

N-Sulphamyl-3-chloropropionamidine Hydrochloride

CAS: 106649-95-0

Applications N-Sulphamyl-3-chloropropionamidine Hydrochloride is used in preparation Famotidine.
References Ballester Rodes, M., et al.: Span., (1989);

Formula: C₃H₈ClN₃O₂S·HCl

Color and Shape: White To Off-White

Molecular weight: 185.63 + (36.46)

Ref: TR-N223595

N-Sulphamyl-3-chloropropionamidine hydrochloride

CAS: 106649-95-0

N-Sulphamyl-3-chloropropionamidine hydrochloride is a chemical compound that is used as a stain for histological studies. It is activated by chloride ions and reacts with cellular components in tissue sections to form a black precipitate. This technique is used for the diagnosis of tuberculosis and other bacterial infections. A number of techniques are available for this staining, including potassium dichromate, mercuric chloride, and rotator methods. Other uses include the identification of histologists or tissues.

Formula: C₃H₈ClN₃O₂S•HCl

Color and Shape: Powder

Molecular weight: 222.09 g/mol

Ref: 3D-FS35072

3-Chloro-N-sulfamoylpropanimidamide hydrochloride

CAS: 106649-95-0

Purity: 95%

Molecular weight: 222.0800018

Ref: 10-F867883

3-Chloro-N-sulfamoylpropanimidamide

CAS: 106649-95-0

Purity: 97%

Molecular weight: 185.6300049

Ref: 10-F900299