41173-36-8 Usage
Description
1-(4-CHLORO-2-NITROPHENYL)PYRROLIDINE is a chemical compound with the molecular formula C10H11ClN2O2. It is a pyrrolidine derivative that contains a chloro-nitrophenyl group, which gives it potential applications as a building block in organic synthesis. This unique structure and functional groups make it an important molecule for research and development in the chemical and pharmaceutical industries.
Uses
Used in Pharmaceutical Industry:
1-(4-CHLORO-2-NITROPHENYL)PYRROLIDINE is used as a building block for the synthesis of pharmaceutical intermediates due to its chloro-nitrophenyl group. This group can be further modified or reacted to create a variety of compounds with potential therapeutic applications.
Used in Agrochemical Industry:
1-(4-CHLORO-2-NITROPHENYL)PYRROLIDINE is used as a building block for the synthesis of agrochemical intermediates. Its unique structure and functional groups can be utilized to develop new compounds with pesticidal, herbicidal, or other agricultural applications.
Used in Medicinal Chemistry Research:
1-(4-CHLORO-2-NITROPHENYL)PYRROLIDINE serves as a useful tool in medicinal chemistry for the development of new drugs. Its structure can be modified to explore various biological activities, potentially leading to the discovery of novel therapeutic agents.
Used in Organic Synthesis:
1-(4-CHLORO-2-NITROPHENYL)PYRROLIDINE is used as a key intermediate in organic synthesis, allowing chemists to create a wide range of compounds with diverse applications, from pharmaceuticals to specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 41173-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,7 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41173-36:
(7*4)+(6*1)+(5*1)+(4*7)+(3*3)+(2*3)+(1*6)=88
88 % 10 = 8
So 41173-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClN2O2/c11-8-3-4-9(10(7-8)13(14)15)12-5-1-2-6-12/h3-4,7H,1-2,5-6H2
41173-36-8Relevant articles and documents
Specific features of nucleophilic substitution in 1-chloro-3,4- dinitrobenzene
Zotova,Kushakova,Kuznetsov,Rodin,Garabadzhiu
, p. 1473 - 1476 (2007/10/03)
Effects of the solvent, temperature, and nucleophile nature on the selectivity of nucleophilic substitution in 1-chloro-3,4-dinitrobenzene were studied, and optimal conditions were found for the synthesis and isolation of particular products.
Aromatic Nucleophilic Substitution of Halobenzenes with Amines under High Pressure
Ibata, Toshikazu,Isogami, Yasushi,Toyoda, Jiro
, p. 42 - 49 (2007/10/02)
The nucleophilic substitution reactions of aromatic halides having electron-attracting groups on ortho or para position with various primary and secondary amines were accelerated by high pressure to give the corresponding N-substituted anilines in high yields.The bulkiness of amines affects its reactivity to lower the yields of the products.Although the secondary amines are usually less reactive than primary amines, cyclic secondary amines such as morpholine, piperidine, and pyrrolidine were found very reactive. 1,4-Diazabicyclooctane and quinuclidine gave N-quarternary ammonium halides in high yields in contrast to the low reactivity of acyclic tertiary amines.Dichloro- and trichloro-nitrobenzenes also react with diethylamine, pyrrolidine, and morpholine to give mono-, di-, and trisubstitution products depending upon the amount of amine and the position of nitro group in these chlorides.