254731-40-3 Usage
Molecular structure
A derivative of naphthalene with a tetrahydro-1-naphthylamine core structure.
Configuration
The compound has a cis configuration, meaning the chlorine atoms on the phenyl ring are positioned on the same side of the molecule.
Substitution
Contains a methyl group (-CH3) and two chlorine atoms (-Cl) on the phenyl ring.
Salt form
It is a mandelate salt, which is a compound formed by the ionic bond between the tetrahydro-1-naphthylamine and the mandelic acid (2-hydroxy-2-phenylacetic acid).
Potential pharmacological properties
The compound may exhibit various pharmacological properties, making it a potential candidate for use in medicine or pharmacology.
Research and testing
Further research and testing are required to determine the specific uses and applications of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 254731-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,7,3 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 254731-40:
(8*2)+(7*5)+(6*4)+(5*7)+(4*3)+(3*1)+(2*4)+(1*0)=133
133 % 10 = 3
So 254731-40-3 is a valid CAS Registry Number.
254731-40-3Relevant academic research and scientific papers
PROCESS FOR THE MANUFACTURE OF SERTRALINE
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Page 13, (2010/02/05)
Process for the preparation of sertraline by reductive amination of racemic 4-(3, 4-dichlorophenyl)-3, 4-dihydro-1-(2H)-naphthalenone, carried out as one- reaction-vessel process without isolation of intermediates, in the form of pure separated cis and trans isomers, the way of conversion of trans isomer to cis isomer and preparation of FII polymorph of 1S-cis isomer from any other polymorph.
