10305-42-7

Basic information

• Product Name: PROPYLSULFAMOYL CHLORIDE
• Synonyms: PROPYLSULFAMOYL CHLORIDE;n-Propylsulphamoylchloride;n-Propylsulfamoyl chloride
• CAS NO: 10305-42-7
• Molecular Formula: C₃H₈ClNO₂S
• Molecular Weight: 157.62
• Mol File: 10305-42-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 220.4°C at 760 mmHg
• Flash Point: 87.1°C
• Appearance: /
• Density: 1.321g/cm³
• Vapor Pressure: 0.113mmHg at 25°C
• Refractive Index: 1.469
• CAS DataBase Reference: PROPYLSULFAMOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: PROPYLSULFAMOYL CHLORIDE(10305-42-7)
• EPA Substance Registry System: PROPYLSULFAMOYL CHLORIDE(10305-42-7)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 10305-42-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C3H8ClNO2S/c1-2-3-5-8(4,6)7/h5H,2-3H2,1H3

Upstream product

• 51223-95-1 sodium n-propylsulphamate 
• 27238-48-8 N-propylsulfamic acid 
• 556-53-6 N-propylamine hydrochloride 
• 107-10-8 propylamine 

Downstream Products

• 147962-41-2 N-propylaminosulfonamide 
• 1469978-61-7 (rac)-N-[4-(4-cyanophenyl)-5,6,7,8-tetrahydroisoquinolin-8-yl]-N'-propylsulfuric diamide 
• 1186502-70-4 methyl 2,6-difluoro-3-(N-propylsulfamoylamino)benzoate 
• 1084332-51-3 2-[3-[[(propylamino)sulfonyl]amino]phenoxy]-4-fluoro-6-[(2-fluoro-4-iodophenyl)amino]-benzamide 
• 1084332-52-4 2-(3-acetylamino-phenoxy)-4-fluoro-6-(2-fluoro-4-iodo-phenylamino)-benzamide 
• 925891-74-3 N-octadecyl-N'-propylsulfamide 
• 867182-44-3 C₁₁H₁₅ClN₂O₄S 
• 96920-98-8 2-oxo-2-phenyl-N-propylethane-1-sulfonamide 
• 96855-90-2 2-Oxo-cyclohexanesulfonic acid propylamide 
• 26120-11-6 N-Benzyl-N'-propyl-sulfonyldiamid 
• 26120-15-0 N-Cyclohexyl-N'-propyl-sulfonyldiamid 
• 26118-80-9 N-Propyl-amidosulfonsaeure-thiophenylester 
• 26118-72-9 N-Propyl-amidosulfonsaeure-<2-phenoxy-ethylester> 
• 936213-94-4 (C₆H₅)3CSC₄H₆NCO₂CH₂CHCH₂CNOCH₃CH₂NHSO₂NHCH₂CH₂CH₃ 

Relevant articles and documents

Sulfonamides 18 β - glycyrrhetinic acid derivatives and preparation method and application thereof

The invention provides a sulfonamides 18 β - glycyrrhetinic acid derivative as well as a preparation method and application thereof. Belong to medicine technical field. To the invention, the series of derivatives of 18 β - glycyrrhetinic acid modified by sulfonamide groups is designed and synthesized. By introducing an active sulfonamide group, the water solubility and the bioavailability of the compound can be significantly improved to improve the antitumor activity of the related derivative. Experiments prove that the compound 6a has excellent cytotoxic activity for 3 human cancer cells (MCF - 7, A549, HEPG2), is far higher than the parent drug GA, and the activity of the compound 6a in comparison with the positive control anti-cancer drug gefitinib is remarkably improved. The compound is expected to be a prodrug for replacing gefitinib. The drug resistance of the cancer patients to gefitinib can be solved. Thus, the utility model has good practical application value.

2,1,3-Benzothiadiazine derivatives: Synthesis and screening versus PDE4 enzyme

A series of N-1,3 disubstituted 2,1,3-benzothiadiazine derivatives (BTDs) were synthesized and evaluated for their inhibitory activity versus enzymatic isoform PDE4 extracted from U937 cell line. Some of the tested compounds showed a high PDE4 inhibitory activity at 100:μM and the IC50 value of the most interesting terms were evaluated. The structure-activity relationships of these compounds showed that the 3,5-di-tert-butyl-4-hydroxybenzyl moiety at N-1 position is important to obtain activity at micromolar level as previously reported. For the same compounds the antioxidant activity were evaluated highlighting 14 as the most significative one. The introduction of other bulky substituents in N-1 position is detrimental.

N-pyrazinecarbonyl-N'-substituted-sulfamoylguanidine and processes for preparing same

The case involves novel N-pyrazinecarbonyl-N'-substituted-sulfamoylguanidine and processes for preparing same. The N-pyrazinecarbonyl-N'-substituted-sulfamoylguanidines are excellent eukalemic agents possessing diuretic and natriuretic properties.