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CAS:40566-85-6 | 4-HYDRAZINO-BENZOIC ACID ETHYL ESTER HCL

CAS:40566-85-6 | 4-HYDRAZINO-BENZOIC ACID ETHYL ESTER HCL

Molecular Formula:C9H13ClN2O2
Molecular Weigh:216.67
Purity:97%
Package:1g 5g 10g
Worldwide Delivery
Made in China

Product Introduction

Introduction of CAS:40566-85-6 | 4-HYDRAZINO-BENZOIC ACID ETHYL ESTER HCL

 

Ethyl 4-hydrazinylbenzoate hydrochloride, also known as EHBAH, is a synthetic compound used in a variety of scientific research applications. It is a white crystalline powder with a molecular weight of 246.71 g/mol and a melting point of 190-192°C. EHBAH is soluble in water and ethanol and is used for a variety of biochemical and physiological processes.

 

Specification of CAS:40566-85-6 | 4-HYDRAZINO-BENZOIC ACID ETHYL ESTER HCL

 

ITEMS

SPECIFICATION

Purity

97%

Molecular Formula

C9H13ClN2O2

Molecular Weigh

216.67

Storage condition

Inert atmosphere,Room Temperature

 

Research Application of CAS:40566-85-6 | 4-HYDRAZINO-BENZOIC ACID ETHYL ESTER HCL

Photonic Applications

Ethyl 4-hydrazinylbenzoate hydrochloride is explored in the field of photonics. Studies have shown that its derivatives exhibit significant third-order nonlinear optical properties, making them promising for applications in photonic devices. For instance, derivatives like ethyl 2-((2E)-2-(4-(dimethylamino)benzylidene]hydrazinyl)-5-nitrobenzoate exhibit reverse saturable absorption, a property beneficial for optical limiting applications in photonics (Nair et al., 2022).

Material Synthesis and Characterization

Ethyl 4-hydrazinylbenzoate hydrochloride is used in synthesizing and characterizing new materials. For instance, its derivatives have been synthesized and characterized for their optical properties using techniques like single crystal X-ray diffraction and DFT-based studies. These materials have shown significant nonlinear optical (NLO) characteristics, which are important for technological applications (Haroon et al., 2019).

Bioorthogonal Chemistry

In bioorthogonal chemistry, ethyl 4-hydrazinylbenzoate hydrochloride is used to form stable boron-nitrogen heterocycles in neutral aqueous solutions. These reactions are orthogonal to protein functional groups, making them useful for protein conjugation in bioorthogonal coupling reactions under physiologically compatible conditions (Dilek et al., 2015).

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