20852-34-0

Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 4-(benzo[d]oxazol-2-ylaMino)benzoate is used as a building block for the synthesis of various drugs and pharmaceutical products due to its potential pharmacological properties.
Used in Scientific Research:
ethyl 4-(benzo[d]oxazol-2-ylaMino)benzoate is utilized in scientific research for studying its antimicrobial and antifungal activities, contributing to the development of new treatments and therapies.
Used as a Chemical Intermediate in Organic Synthesis:
Ethyl 4-(benzo[d]oxazol-2-ylaMino)benzoate serves as a chemical intermediate, facilitating the creation of complex organic molecules for various applications in the chemical and pharmaceutical industries.
It is crucial to handle ethyl 4-(benzo[d]oxazol-2-ylaMino)benzoate with care, as improper handling and disposal may pose risks to human health and the environment.

InChI:InChI=1/C16H14N2O3/c1-2-20-15(19)11-7-9-12(10-8-11)17-16-18-13-5-3-4-6-14(13)21-16/h3-10H,2H2,1H3,(H,17,18)

Upstream product

• 1205-06-7 4-ethoxycarbonylphenyl isothiocyanate 
• 95-55-6 2-amino-phenol 
• 615-18-9 2-chloro-1,3-benzoxazole 
• 94-09-7 p-aminoethylbenzoate 

Downstream Products

• 20852-35-1 4-(benzo[d]oxazol-2-ylamino)benzoic acid 

Relevant academic research and scientific papers

Microwave-assisted hydrogen peroxide-mediated synthesis of benzoxazoles and related heterocycles via cyclodesulfurization

A novel approach has been developed to construct benzoxazoles and similar N- and S-containing heterocycles from their corresponding isothiocyanates and o-substituted anilines via cyclodesulfurization. The reaction was found to proceed via in situ formatio

Electrochemical NaI/NaCl-mediated one-pot synthesis of 2-aminobenzoxazoles in aqueous mediaviatandem addition-cyclization

An electrochemical synthesis of 2-aminobenzoxazoles from 2-aminophenols and isothiocyanates was successfully developed in a one-pot fashion. Using inexpensive and widely available NaI and NaCl co-operatively in catalytic amounts, our electrosynthesis approach provided various 2-aminobenzoxazole products in moderate to high yields in an open-flask type undivided cell without using any external supporting electrolyte and base. The protocol can be applied to the synthesis of 2-aminobenzothiazoles from the corresponding 2-thiophenols in moderate yields. This protocol has many benefits. It is metal-free and highly scalable and uses inexpensive mediators and EtOH/water as an environmentally friendly solvent under mild conditions.

Selectively targeting T- and B-cell lymphomas: A benzothiazole antagonist of α4β1integrin

Current cancer chemotherapeutic agents clinically deployed today are designed to be indiscriminately cytotoxic, however, achieving selective targeting of cancer malignancies would allow for improved diagnostic and chemotherapeutic tools. Integrin α4β1, a heterodimeric cell surface receptor, is believed to have a low- affinity conformation in resting normal lymphocytes and an activated high-affinity conformation in cancerous cells, specifically T- and B-cell lymphomas. This highly attractive yet poorly understood receptor has been selectively targeted with the bisaryl urea peptidomimetic antagonist i. However, concerns regarding its preliminary pharmacokinetic (PK) profile provided an impetus to change the pharmacophore from a bisaryl urea to a 2-arylaminobenzothiazole moiety, resulting in an analogue with improved physicochemical properties, solubility, and kidney:tumor ratio while maintaining potency (6;IC50 = 53 pM). The results presented herein utilized heterocyclic and solid-phase chemistry, cell adhesion assay, and in vivo optical imaging using the cyanine dye Cy5.5 conjugate.