62129-02-6

Basic information

• Product Name: 4-AMINO-2-BENZOOXAZOL-2-YL-PHENOL
• Synonyms: 4-AMINO-2-(1,3-BENZOXAZOL-2-YL)PHENOL;4-AMINO-2-BENZOOXAZOL-2-YL-PHENOL;AKOS BB-8259;LABOTEST-BB LT00133909;ASISCHEM T30911;ART-CHEM-BB B025294;TIMTEC-BB SBB000660
• CAS NO: 62129-02-6
• Molecular Formula: C₁₃H₁₀N₂O₂
• Molecular Weight: 226.23
• Mol File: 62129-02-6.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-AMINO-2-BENZOOXAZOL-2-YL-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINO-2-BENZOOXAZOL-2-YL-PHENOL(62129-02-6)
• EPA Substance Registry System: 4-AMINO-2-BENZOOXAZOL-2-YL-PHENOL(62129-02-6)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 62129-02-6(Hazardous Substances Data)

Usage

General Description

4-Amino-2-benzooxazol-2-yl-phenol, also known as ABOP, is a chemical compound that belongs to the class of benzooxazoles. It is an important intermediate in the synthesis of pharmaceuticals and other organic compounds. ABOP is used in the production of various drugs, such as anti-inflammatory and antibacterial agents. It is also used as a building block in the synthesis of dyes and pigments. ABOP has a range of applications in the pharmaceutical and chemical industries, making it a versatile and valuable compound in organic synthesis.

Upstream product

• 89-57-6 5-Aminosalicylic Acid 
• 95-55-6 2-amino-phenol 
• 60344-96-9 2-(2′-hydroxy-5′-nitrophenyl)-1,3-benzoxazole 

Downstream Products

• 2533-08-6 C₁₅H₁₂N₂O₃ 
• 1422453-81-3 C₂₃H₂₈N₂O₃ 
• 1609074-41-0 2-(5'-N-octylamino-2'-hydroxyphenyl)benzoxazole 
• 1609074-40-9 2-(5-N-dodecylamino-2-hydroxyphenyl)benzoxazole 
• 1609074-38-5 2-(5-(N-3-chloro-2-hydroxypropylamino)-2-hydroxyphenyl)benzoxazole 
• 1149804-19-2 2-[5’-(N-4,6-dichloro-1,3,5-triazin-2-yl)-2’-hydroxyphenyl]benzoxazole 
• 1312023-88-3 C₁₇H₁₂N₂O₄ 

Relevant articles and documents

A simple excited-state intramolecular proton transfer probe based on a new strategy of thiol-azide reaction for the selective sensing of cysteine and glutathione

A simple azido-substituted fluorescent sensor AHBO showing a selective turn-on response to cysteine (Cys) and glutathione (GSH) over homocysteine (Hcy), sulfide and other amino acids has been constructed, which is based on the mechanism of selective nucle

Proton-Transfer-Based Azides with Fluorescence Off-On Response for Detection of Hydrogen Sulfide: An Experimental, Theoretical, and Bioimaging Study

This work describes the synthesis of photoactive proton transfer compounds based on the benzazolic core containing the azide group. The compounds present absorption in the UV region and fluorescence emission in the visible region of the spectra with large

Synthesis, characterization and photophysics of new photoactive esipt lipophilic dyes. partition experiments with different composed liposomes

New lipophilic dyes were synthesized from a fluorescent precursor and used to produce photoactive liposomes and ethosomes made of different phospholipids. The lipophilic dyes absorbed in the ultraviolet region due to π-π* transitions and had a dual fluorescence emission in the violet-yellow regions, depending on solvent polarity. The long alkyl chain lipophilic dyes had a narrow emission band with a very regular shape, and their photophysical behaviour indicates that these dyes were inserted into the lipid bilayer. The dye with short alkyl chain appeared to be in a polar environment, which indicated this fluorophore experienced a more hydrophobic environment. Fluorescence titration experiments were also performed with this compound and the partition coefficient was determined, which showed higher values than those found in the literature for similar intramolecular proton transfer dyes, likely due to better interaction between this dye and the phospholipids, due to the alkyl chain present in the dyes.