73948-18-2 Usage
Uses
Used in Organic Synthesis:
4-(N-Pentyl)benzenesulfonyl chloride is used as a reagent in the field of organic synthesis for the preparation of various chemical compounds. Its sulfonyl chloride group allows it to participate in a range of chemical reactions, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(N-Pentyl)benzenesulfonyl chloride is used as a building block for the synthesis of drug molecules. Its unique structure and reactivity enable the creation of new compounds with potential therapeutic applications, contributing to the development of novel medications.
Used in Research Applications:
4-(N-Pentyl)benzenesulfonyl chloride is used as a research tool in academic and industrial laboratories. It serves as a model compound for studying the properties and reactions of sulfonyl chlorides, providing insights into their behavior and potential applications in various chemical processes.
Used in Chemical Intermediates Production:
4-(N-Pentyl)benzenesulfonyl chloride is used as a key intermediate in the production of other chemical compounds. Its versatility in undergoing various chemical transformations makes it an essential component in the synthesis of a wide range of products, including specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 73948-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,4 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73948-18:
(7*7)+(6*3)+(5*9)+(4*4)+(3*8)+(2*1)+(1*8)=162
162 % 10 = 2
So 73948-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15ClO2S/c1-2-3-4-5-10-6-8-11(9-7-10)15(12,13)14/h6-9H,2-5H2,1H3
73948-18-2Relevant academic research and scientific papers
Huang, Zhangjian,Velazquez, Carlos,Abdellatif, Khaled,Chowdhury, Morshed,Jain, Sarthak,Reisz, Julie,Dumond, Jenna,King, S. Bruce,Knaus, Edward
, p. 4124 - 4130 (2010)
Nitric oxide (NO) and its reduced form nitroxyl (HNO), effective vasodilation agents that can inhibit platelet aggregation and adhesion, could suppress adverse cardiovascular effects associated with the use of selective COX-2 inhibitors. In this regard, a
Catalytic Properties of Carbonyl Reductase from Rabbit Kidney for Acetohexamide and Its Analogs
Imamura, Yorishige,Higuchi, Toshiyuki,Otagiri, Masaki,Nagumo, Shinji,Akita, Hiroyuki
, p. 387 - 394 (2007/10/02)
Analogs submitted by ethyl, n-propyl, n-butyl, and isopropyl groups instead of methyl group adjacent to a ketone group of acetohexamide were synthesized and the structural requirements of carbonyl reductase from rabbit kidney for these analogs were kineti
4-Substituted phenyl 4'-(5-N-alkyl-1,3-dioxan-2-yl) thiobenzoates
-
, (2008/06/13)
Disclosed are compounds of the formula: STR1 wherein R1 is an alkyl group having 1 to 10 carbon atoms and R2 is either an alkyl or alkoxy group having 1 to 10 carbon atoms or a cyano group or a nitro group. The compounds of the inven
