75333-04-9 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(4-chlorobenzyl)hydrazine dihydrochloride is used as a building block and reagent in the synthesis of various pharmaceuticals and organic compounds. Its unique structure and properties make it a valuable component in the development of new drugs and chemical entities.
Used in Research and Laboratory Settings:
In research and laboratory settings, 1-(4-chlorobenzyl)hydrazine dihydrochloride is used for its potential applications in the treatment of tuberculosis and other microbial infections. Its inhibitory effects on cell wall biosynthesis make it a promising candidate for the development of new antimicrobial agents.
Used in Microbial Infection Treatment:
1-(4-chlorobenzyl)hydrazine dihydrochloride is used as an antimicrobial agent for the treatment of tuberculosis and other microbial infections. Its ability to inhibit cell wall biosynthesis in microorganisms contributes to its effectiveness in combating these infections.
Used in Safety and Handling Protocols:
Due to its potential hazards, 1-(4-chlorobenzyl)hydrazine dihydrochloride is used in the development of safety and handling protocols to ensure its safe use in research, laboratory, and pharmaceutical settings. Proper handling and adherence to safety guidelines are essential to minimize risks associated with 1-(4-chlorobenzyl)hydrazine dihydrochloride.
Check Digit Verification of cas no
The CAS Registry Mumber 75333-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,3 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75333-04:
(7*7)+(6*5)+(5*3)+(4*3)+(3*3)+(2*0)+(1*4)=119
119 % 10 = 9
So 75333-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H9ClN2.ClH/c8-7-3-1-6(2-4-7)5-10-9;/h1-4,10H,5,9H2;1H
75333-04-9Relevant academic research and scientific papers
N-Amino-1,8-Naphthalimide is a Regenerated Protecting Group for Selective Synthesis of Mono-N-Substituted Hydrazines and Hydrazides
Manoj Kumar, Mesram,Venkataramana, Parikibanda,Yadagiri Swamy, Parikibanda,Chityala, Yadaiah
supporting information, p. 17713 - 17721 (2021/11/10)
A new route to synthesis of various mono-N-substituted hydrazines and hydrazides by involving in a new C?N bond formation by using N-amino-1,8-naphthalimide as a regenerated precursor was invented. Aniline and phenylhydrazines are reproduced upon reacting these individually with 1,8-naphthalic anhydride followed by hydrazinolysis. The practicality and simplicity of this C?N dihalo alkanes; developed a synthon for bond formation protocol was exemplified to various hydrazines and hydrazides. N-amino-1,8-naphthalimide is suitable synthon for transformation for selective formation of mono-substituted hydrazine and hydrazide derivatives. Those are selective mono-amidation of hydrazine with acid halides; mono-N-substituted hydrazones from aldehydes; synthesis of N-aminoazacycloalkanes from acetohydrazide scaffold and inserted to hydroxy derivatives; distinct synthesis of N,N-dibenzylhydrazines and N-benzylhydrazines from benzyl halides; synthesis of N-amino-amino acids from α-halo esters. Ecofriendly reagent N-amino-1,8-naphthalimide was regenerated with good yields by the hydrazinolysis in all procedures.
