5983-84-6 Usage
Molecular structure
2-(2-aminoethyl)-3-(4-chlorophenyl)-3-hydroxy-2,3-dihydro-1H-isoindol-1-one has a complex molecular structure with an aminoethyl group, a chlorophenyl group, and a hydroxy group attached to an isoindol-1-one ring.
Aminoethyl group
The presence of an aminoethyl group (-NH2CH2CH2-) contributes to the compound's basic character and provides the potential for hydrogen bonding and coordination with other molecules.
Chlorophenyl group
The 4-chlorophenyl group (-C6H4Cl) imparts lipophilicity and may contribute to the compound's ability to cross cell membranes and interact with specific targets in the body.
Hydroxy group
The hydroxy group (-OH) adds polarity to the molecule, which can influence solubility, stability, and the compound's ability to form hydrogen bonds with other molecules.
Potential pharmaceutical agent
2-(2-aminoethyl)-3-(4-chlorophenyl)-3-hydroxy-2,3-dihydro-1H-isoindol-1-one has potential applications in the pharmaceutical industry, particularly as a drug for the treatment of neurological disorders, psychiatric conditions, or as an analgesic.
Further research and testing
The specific properties and potential uses of 2-(2-aminoethyl)-3-(4-chlorophenyl)-3-hydroxy-2,3-dihydro-1H-isoindol-1-one would need to be investigated through additional research and testing to determine its safety, efficacy, and optimal therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5983-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,8 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5983-84:
(6*5)+(5*9)+(4*8)+(3*3)+(2*8)+(1*4)=136
136 % 10 = 6
So 5983-84-6 is a valid CAS Registry Number.
5983-84-6Relevant academic research and scientific papers
Maulding,Turi,Grossman,Nazareno
, p. 1833 - 1838 (1975)
Hydrolysis of mazindol to form 2 (2 aminoethyl) 3 (p chlorophenyl) 3 hydroxyphthalimidine was followed spectrophotometrically in aqueous solutions at temperatures between 37 and 70°, pH values up to 7.6, and an ionic strength of 0.2. The effects of acetate, formate, and phosphate buffers as well as ionic strength on the observed rate constants were investigated. An interesting nonlinear dependency of the k(obs) with buffer concentration was noted. The velocity constants declinded with increasing hydrogen ion concentration; the log k pH profile and rate law are given along with other relevant data.
Imidazolinyl phenyl carbonyl compounds acid addition salts and related compounds
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, (2008/06/13)
This invention is concerned with tetrahydropyrimidinyl phenyl carbonyl acid addition salts, imidazolinyl phenyl carbonyl acid addition salts, dihydroimidazoisoindolols, tetrahydropyrimidoisoindolols, and tetrahydropyrimidoisoindolol acid addition salts which are all pharmacologically efficacious as anti-depressants. The tetrahydropyrimidinyl phenyl carbonyl acid addition salts, the tetrahydropyrimidoisoindolols and the tetrahydropyrimidoisoindolol acid addition salts are also efficacious as diuretics while the imidazolinyl phenyl carbonyl acid addition salts and the dihydroimidazoisoindolols are efficacious as anorexiants. This invention is also concerned with several processes for the preparation of these compounds.
