146949-07-7 Usage
Description
4-N-Propylbenzenesulfonyl chloride, an R-arylsulfonyl chloride, is an organic compound with the molecular formula C10H11ClO2S. It is a derivative of benzene with a sulfonyl chloride group attached to the 4-position and a propyl group attached to the nitrogen atom. 4-N-PROPYLBENZENESULFONYL CHLORIDE is known for its reactivity and is commonly used as an intermediate in the synthesis of various organic compounds.
Uses
Used in Chemical Synthesis:
4-N-Propylbenzenesulfonyl chloride is used as a synthetic intermediate for the production of various organic compounds. Its reactivity allows it to be a key component in the synthesis of different molecules, making it valuable in the field of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-N-Propylbenzenesulfonyl chloride is used as a building block for the development of new drugs. Its unique structure and reactivity enable the creation of novel drug candidates with potential therapeutic applications.
Used in Synthesis of Sodium 4n-Propylbenzenesulfonate:
4-N-Propylbenzenesulfonyl chloride is used as a starting material in the synthesis of sodium 4n-propylbenzenesulfonate. 4-N-PROPYLBENZENESULFONYL CHLORIDE has various applications, including its use as a chemical intermediate and in the production of other organic compounds.
Used in Synthesis of N-(2-Aminophenyl)arylsulfonamide:
4-N-Propylbenzenesulfonyl chloride is also utilized in the synthesis of N-(2-aminophenyl)arylsulfonamide, a compound with potential applications in the pharmaceutical and chemical industries. Its role in this synthesis highlights its versatility as a synthetic intermediate.
Check Digit Verification of cas no
The CAS Registry Mumber 146949-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 146949-07:
(8*1)+(7*4)+(6*6)+(5*9)+(4*4)+(3*9)+(2*0)+(1*7)=167
167 % 10 = 7
So 146949-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11ClO2S/c1-2-3-8-4-6-9(7-5-8)13(10,11)12/h4-7H,2-3H2,1H3
146949-07-7Relevant articles and documents
Guanidine compound for preventing and treating chronic pain medication (by machine translation)
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Paragraph 0133-0139, (2020/08/27)
The invention relates to a guanidine compound as shown in general formula (I) as a guanidine compound for preventing and treating chronic pain disease. A pharmaceutically acceptable salt thereof, a prodrug thereof, a solvate thereof, a deuterated substanc
Bispiperidines as antithrombotic agents
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, (2008/06/13)
Novel compounds which are inhibitors of the binding of fibrinogen to the Gp IIb/IIIa platelet receptors, and which can be used therepeutically as antithrombotic agents
Antibacterially Active Substituted Anilides of Carboxylic and Sulfonic Acids
Linfield, Warner M.,Micich, Thomas J.,Montville, Thomas J.,Simon, John R.,Murray, Ermellina B.,Bistline, Raymond G.
, p. 1741 - 1746 (2007/10/02)
Anilides of carboxylic and sulfonic acids were prepared and tested for antimicrobial activity.While these anilides were ineffective against Gram-negative organisms, there was good correlation between chemical structure and biological activity against Gram-positive species.Both the nature and position of the benzene ring substituents and the length of the carbon side chain affected the activity and specificity of the compounds.The highest activity was observed when the acyl or sulfuryl moiety had a C7-C9 side chain attached.The CONH and SO2NH bridging groups wereequally effective.The attachment of COOH or COOCH3 groups in the ω-position did not effect activity, but the substitution of the acidic proton of the sulfonamide group by an alkyl group rendered the compound inactive.Six compounds, which were substituted anilides of sulfonic acids, fatty acids, or the analogues α-methylene-substituted acids, were bacteriostatic at 10 ppm against Bacillus cereus, Staphylococcus aureus, Streptococcus faecalis and Lactobacillus plantarum .One of these compounds, 2-hydroxy-5-nitroanilide of α-methylenedecanoic acid, was bactericidal at 1 ppm.