27483-92-7 Usage
Uses
Used in Pharmaceutical Industry:
N-(2-Chloromethyl)-N-methylpiperidine, hydrochloride salt is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Chemical Synthesis:
In the field of organic chemistry, N-(2-Chloromethyl)-N-methylpiperidine, hydrochloride salt is used as a reactant in chemical reactions. Its reactivity and functional groups make it a valuable building block for the creation of complex organic molecules.
Used in Research and Development:
N-(2-Chloromethyl)-N-methylpiperidine, hydrochloride salt is utilized in research laboratories for the development of new chemical processes and the exploration of its potential applications in various chemical and biological systems. Its stability and solubility properties facilitate its use in experimental procedures.
Used in Fine Chemicals Production:
N-(2-Chloromethyl)-N-methylpiperidine, hydrochloride salt is employed as an intermediate in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, agriculture, and materials science. Its role in this context is crucial for the synthesis of specialty chemicals with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 27483-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,8 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27483-92:
(7*2)+(6*7)+(5*4)+(4*8)+(3*3)+(2*9)+(1*2)=137
137 % 10 = 7
So 27483-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H14ClN.ClH/c1-9-5-3-2-4-7(9)6-8;/h7H,2-6H2,1H3;1H
27483-92-7Relevant articles and documents
Potent cannabinergic indole analogues as radioiodinatable brain imaging agents for the CB1 cannabinoid receptor
Deng, Hongfeng,Gifford, Andrew N.,Zvonok, Alexander M.,Cui, Guangjian,Li, Xiuyan,Fan, Pusheng,Deschamps, Jeffrey R.,Flippen-Anderson, Judith L.,Gatley, S. John,Makriyannis, Alexandros
, p. 6386 - 6392 (2007/10/03)
A series of novel aminoalkylindoles was synthesized in an effort to develop compounds that are potent agonists at the CB1 cannabinoid receptor and that are also easily labeled with radioisotopes of iodine for biochemical and imaging studies. 2-Iodophenyl-
Substituted anilino-quinazoline (or quinoline) compounds and use thereof
-
, (2008/06/13)
The invention concerns amide derivatives of Formula (I), wherein: G is N or CH; R1is a group such as hydroxy, halo, trifluoromethyl, C1-6alkyl and C1-6alkoxy; each of R2and R3is hydrogen, halo, C1-6alkyl, C2-6alkenyl or C2-6alkynyl; R4is a group such as hydrogen, hydroxy, C1-6alkyl, C1-6alkoxy and C3-7cycloalkyl, or R4is of the Formula (IC): —K—J, wherein J is aryl, heteroaryl or heterocyclyl and K is a bond or a group such as oxy and imino, R5is a group such as hydrogen, halo and trifluoromethyl: m is 1-3 and q is 0-4; or pharmaceutically acceptable salts or in vivo cleavable esters thereof; processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of diseases or medical conditions mediated by cytokines.
