29519-77-5

Basic information

• Product Name: (4-Hydrazinophenyl)acetic acid
• Synonyms: (4-Hydrazinophenyl)acetic acid
• CAS NO: 29519-77-5
• Molecular Formula: C₈H₁₀N₂O₂
• Molecular Weight: 166.18
• Product Categories: Carboxylic Acids;Phenyls & Phenyl-Het
• Mol File: 29519-77-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 174-175.5 °C (decomp)
• Boiling Point: 388.6±25.0 °C(Predicted)
• Appearance: /
• Density: 1.345±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 4.26±0.10(Predicted)
• CAS DataBase Reference: (4-Hydrazinophenyl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-Hydrazinophenyl)acetic acid(29519-77-5)
• EPA Substance Registry System: (4-Hydrazinophenyl)acetic acid(29519-77-5)

Safety Data

• Hazardous Substances Data: 29519-77-5(Hazardous Substances Data)

Usage

Description

(4-Hydrazinophenyl)acetic acid, with the molecular formula C8H10N2O2, is an aromatic hydrazine derivative featuring a carboxylic acid functional group. This chemical compound holds promise for various applications due to its unique structure and properties.

Uses

Used in Pharmaceutical Industry:
(4-Hydrazinophenyl)acetic acid is used as a pharmaceutical intermediate for the synthesis of various drugs. Its aromatic hydrazine and carboxylic acid functional groups make it a versatile building block in the development of new pharmaceutical compounds.
Used in Chemical Synthesis:
In the chemical synthesis industry, (4-Hydrazinophenyl)acetic acid serves as a reagent, contributing to the creation of a wide range of chemical products. Its unique structure allows for its use in multiple reaction pathways, enhancing the diversity of synthesized compounds.
Used in Medicinal Research:
(4-Hydrazinophenyl)acetic acid is used as a subject of study in medicinal research due to its potential biological activities. Further investigation into its properties may lead to the discovery of new therapeutic applications, particularly in the development of treatments for various diseases.
Used in Biological Research:
As a compound with demonstrated biological activities, (4-Hydrazinophenyl)acetic acid is also utilized in biological research. It may play a role in understanding certain biological processes or serve as a tool to probe the mechanisms of specific biological systems.

Upstream product

• 1197-55-3 4-aminophenylacetic acid 

Relevant articles and documents

Dye compounds

The present invention relates to dye compounds represented by Formulae I and II, which are described in the specification. The dye compounds of the present invention have markedly improved quantum yields and emit strong fluorescence compared to existing cyanine dyes. Due to these advantages, the dye compounds of the present invention can find applications in various fields, for example, as probes for various biological systems where optical imaging is required. Particularly, the dye compounds of the present invention can be used as mitotrackers capable of labeling and tracking mitochondria. Therefore, the dye compounds of the present invention can be used to quantitatively image mitochondria in live tissues and cells. Furthermore, the dye compounds of the present invention can be applied as pH probes for measuring the pH of live cells.

Rigidized trimethine cyanine dyes

Disclosed are analogues of trimethine cyanine dyes which are useful for imparting fluorescent properties to target materials by covalent and non-covalent association. The compounds have the following general formula: optionally substituted by groups R2-R9 wherein groups R6, R7, R8 and R9 are attached to the rings containing X and Y or, optionally are attached to atoms of the Za and Zb ring structures and groups R1-R9 are chosen to provide desired solubility, reactivity and spectral properties to the fluorescent compounds; A is selected from O, S and NR11 where R11 is the substituted amino radical: where R′ is selected from hydrogen, a C1-4 alkyl and aryl and R″ is selected from C1-18 alkyl, aryl, heteroaryl, an acyl radical having from 2-7 carbon atoms, and a thiocarbamoyl radical; Za and Zb each represent a bond or the atoms necessary to complete one, two fused or three fused aromatic rings each ring having five or six atoms, selected from carbon atoms and, optionally, no more than two oxygen, nitrogen and sulphur atoms.