64415-10-7 Usage
Description
N-(O-Chlorobenzyl)hydrazide dihydrochloride is a chemical compound characterized by the presence of a hydrazide functional group attached to a chlorobenzyl group. N-(O-CHLOROBENZYL)HYDRAZIDE DIHYDROCHLORIDE is known for its stability and solubility due to its dihydrochloride form, which facilitates its use in a range of research and industrial applications.
Uses
Used in Organic Synthesis:
N-(O-Chlorobenzyl)hydrazide dihydrochloride is utilized as an intermediate in organic synthesis for the development of various chemical compounds and pharmaceuticals. Its unique structure allows it to participate in a variety of chemical reactions, making it a valuable component in the synthesis of new molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-(O-Chlorobenzyl)hydrazide dihydrochloride is used as a starting material for the development of potential antitubercular and antimalarial agents. Its ability to be modified and incorporated into different molecular structures makes it a promising candidate for the creation of new drugs to combat these diseases.
Used in Disease Treatment Research:
N-(O-Chlorobenzyl)hydrazide dihydrochloride has been investigated for its potential use in the treatment of various diseases, including cancer and autoimmune disorders. Its versatility and reactivity in chemical reactions enable researchers to explore its therapeutic properties and possible applications in medicine.
Used in Research and Development:
Due to its stability and solubility, N-(O-Chlorobenzyl)hydrazide dihydrochloride is commonly used in research and development laboratories. It serves as a reliable compound for testing new chemical reactions, exploring its properties, and developing innovative applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 64415-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,1 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64415-10:
(7*6)+(6*4)+(5*4)+(4*1)+(3*5)+(2*1)+(1*0)=107
107 % 10 = 7
So 64415-10-7 is a valid CAS Registry Number.
64415-10-7Relevant articles and documents
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.
