1603-85-6 Usage
Uses
Used in Organic Synthesis:
4-(2,4-DINITROBENZYL)PYRIDINE is used as a protecting group for alcohols and amines in organic synthesis. It reacts with these functional groups through the dinitrobenzyl moiety, forming stable adducts and protecting the primary functionality. This allows chemists to carry out reactions without affecting the alcohol or amine groups, and once the desired reaction is completed, the protecting group can be removed using appropriate conditions, enabling the selective deprotection of the functional groups.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(2,4-DINITROBENZYL)PYRIDINE is used as a key intermediate in the synthesis of various drug molecules. Its ability to protect functional groups during the synthesis process ensures that the final drug product retains the desired chemical properties and biological activity.
Used in Research and Development:
4-(2,4-DINITROBENZYL)PYRIDINE is also used in research and development settings, where it serves as a valuable tool for studying the reactivity and selectivity of various functional groups in complex organic molecules. This helps researchers to better understand the underlying chemical mechanisms and develop new synthetic strategies for the preparation of novel compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1603-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1603-85:
(6*1)+(5*6)+(4*0)+(3*3)+(2*8)+(1*5)=66
66 % 10 = 6
So 1603-85-6 is a valid CAS Registry Number.
1603-85-6Relevant academic research and scientific papers
Vicarious nucleophilic substitution of (chloroalkyl)heterocycles with nitroarenes
Florio, Saverio,Lorusso, Patrizia,Luisi, Renzo,Granito, Catia,Ronzini, Ludovico,Troisi, Luigino
, p. 2118 - 2124 (2007/10/03)
The vicarious nucleophilic substitution of potassium carbanions of the (chloromethyl)pyridines 1a and 1b, (chloromethyl)benzothiazole 1c, (chloromethyl)thiazole 1d, (chloroethyl)thiazole 1e and (chloroethyl) benzothiazole 1f wit nitroarenes, leading to ni
