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Benzoic acid, 4-azido-, hydrazide is a chemical compound with the formula C7H6N6O2. It is a derivative of benzoic acid and contains both azide and hydrazide functional groups. Benzoic acid, 4-azido-, hydrazide has potential applications in the fields of chemistry and pharmacology, as well as in the synthesis of other chemical compounds. Due to its potential health and safety risks, it is important to handle and store benzoic acid, 4-azido-, hydrazide with caution.

63296-32-2

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63296-32-2 Usage

Uses

Used in Chemical Synthesis:
Benzoic acid, 4-azido-, hydrazide is used as a chemical intermediate for the synthesis of other chemical compounds. Its unique azide and hydrazide functional groups make it a versatile building block in organic chemistry.
Used in Pharmaceutical Research:
In the field of pharmacology, benzoic acid, 4-azido-, hydrazide is used as a research compound to explore its potential therapeutic properties. Its structure and functional groups may contribute to the development of new drugs and pharmaceutical agents.
Used in Chemical Reactions:
Benzoic acid, 4-azido-, hydrazide is used as a reactant in various chemical reactions, such as click chemistry, where the azide group can participate in cycloaddition reactions with alkynes to form triazoles. This property allows for the creation of new compounds and materials with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 63296-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,9 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63296-32:
(7*6)+(6*3)+(5*2)+(4*9)+(3*6)+(2*3)+(1*2)=132
132 % 10 = 2
So 63296-32-2 is a valid CAS Registry Number.

63296-32-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-azidobenzohydrazide

1.2 Other means of identification

Product number -
Other names 4-AZIDOBENZOYL HYDRAZINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:63296-32-2 SDS

63296-32-2Downstream Products

63296-32-2Relevant academic research and scientific papers

Biodegradable magnetic nanocarrier for stimuli responsive drug release

Ganivada, Mutyala Naidu,Rao N, Vijayakameswara,Dinda, Himadri,Kumar, Pawan,Das Sarma, Jayasri,Shunmugam, Raja

, p. 2703 - 2711 (2014/05/06)

Biocompatible nanocarriers conjugated with magnetic nanoparticle, doxorubicin and poly(ethylene oxide) (PEG) motif have been designed (PVLPEG-PVLDOXI-PCL-PHOS) to create a magnetic vector under magnetic field. Acylhydrazine linker is used to release the drug exactly at the mild acidic conditions resembling the pH of the cancerous cells. All the monomers and polymers are characterized carefully by the routine analytical techniques. Thermogravimetric analysis (TGA), FT-IR spectroscopy and scanning electron microscope (SEM) techniques are employed to confirm the anchoring of iron particle (Fe3O4) to the PVLPEG-PVLDOXI-PCL-PHOS. Reservoir capabilities of the newly designed biodegradable nanocarrier are tested by both dynamic light scattering (DLS) and transmission electron microscopy (TEM). Drug release profile from nanocarrier is monitored by fluorimeter. The release profile shows the importance of having the acylhydrazine linker that helps to release the drug at the mild acidic conditions similar to cancerous cells. Confocal laser scanning microscopy (CLSM) and flow cytometry studies on 4T cells indicate that nanocarriers from PVLPEG-PVLDOXI-PCL-PHOS polymer are internalized efficiently. It is very interesting to note that the nanocarriers have exhibited both biologically and magnetically targeting abilities toward 4T cells in vitro.

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