82588-29-2 Usage
Class
Quaternary ammonium compounds
Organic salt
Cyclobutane ring
Trimethylammonium group
High melting point
Soluble in water
Industrial and laboratory applications
Used as a reactant in organic synthesis
Used as a catalyst in chemical reactions
Studied for potential use in pharmaceuticals
Studied as an antimicrobial agent
Check Digit Verification of cas no
The CAS Registry Mumber 82588-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,8 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82588-29:
(7*8)+(6*2)+(5*5)+(4*8)+(3*8)+(2*2)+(1*9)=162
162 % 10 = 2
So 82588-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H18NO2.HI/c1-7(11)12-9-6-5-8(9)10(2,3)4;/h8-9H,5-6H2,1-4H3;1H/q+1;/p-1/t8-,9+;/m1./s1
82588-29-2Relevant articles and documents
(+/-)-cis-2-Acetoxycyclobutyltrimethylammonium Iodide: A Semirigid Analogue of Acetylcholine
Cannon, Joseph G.,Crockatt, Dale M.,Long, John Paul,Maixner, William
, p. 1091 - 1094 (2007/10/02)
The title compound was prepared to complete a series of small ring (cyclopropane, cyclobutane) cis/trans 1,2-disubstituted semirigid congeners of acetylcholine.A multistep synthetic sequence, beginning with cis-cyclobutane-1,2-dicarboxylic anhydride, permitted unequivocal preparation of the (+/-)-cis target compound 4.The geometry of 4 was confirmed by comparison with an authentic sample of the (+/-)-trans isomer.The cis and trans isomers were equipotent as muscarinic agonists, but they were much weaker than acetyl-β-methylcholine.
