151255-80-0

Basic information

• Product Name: Methyl 2,4-Bis(benzyloxy)phenylacetate
• Synonyms: Methyl 2,4-Bis(benzyloxy)phenylacetate;methyl 2-(2,4-bis(benzyloxy)phenyl)acetate
• CAS NO: 151255-80-0
• Molecular Formula: C₂₃H₂₂O₄
• Molecular Weight: 362.41838
• Mol File: 151255-80-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 2,4-Bis(benzyloxy)phenylacetate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2,4-Bis(benzyloxy)phenylacetate(151255-80-0)
• EPA Substance Registry System: Methyl 2,4-Bis(benzyloxy)phenylacetate(151255-80-0)

Safety Data

• Hazardous Substances Data: 151255-80-0(Hazardous Substances Data)

Usage

Description

Methyl 2,4-Bis(benzyloxy)phenylacetate is an organic compound that is characterized by its unique chemical structure and properties. It is a derivative of phenylacetate, featuring two benzyloxy groups attached to the 2,4-positions of the phenyl ring. Methyl 2,4-Bis(benzyloxy)phenylacetate is known for its potential applications in various fields due to its specific chemical reactivity and structural features.

Uses

Used in Pharmaceutical Industry:
Methyl 2,4-Bis(benzyloxy)phenylacetate is used as a reactant in the synthesis of fluorescent labeled analogs of spider toxin, NPTX-594. This application is significant because it allows for the development of new tools and techniques in the study of spider toxins, which can have potential therapeutic applications in the future.
In the field of pharmaceuticals, Methyl 2,4-Bis(benzyloxy)phenylacetate serves as a key intermediate in the synthesis of various bioactive compounds. Its unique structure enables it to be a versatile building block for the development of new drugs with specific targeting properties.
Additionally, Methyl 2,4-Bis(benzyloxy)phenylacetate may also find use in the development of novel drug delivery systems, where its chemical properties can be exploited to improve the efficacy and bioavailability of therapeutic agents.

Upstream product

• 67-56-1 methanol 
• 22877-01-6 2,4-bis(benzyloxy)acetophenone 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 100-39-0 benzyl bromide 

Downstream Products

• 66056-40-4 2-(2,4-bis(benzyloxy)phenyl)acetic acid 
• 113978-98-6 dibenzyl-2,4-dihydroxyphenylacetic acid N-hydroxysuccinimide ester 
• 177906-37-5 (3-Azido-propyl)-[2-(5-{(S)-2-[2-(2,4-bis-benzyloxy-phenyl)-acetylamino]-3-carbamoyl-propionylamino}-pentylcarbamoyl)-ethyl]-carbamic acid benzyl ester 
• 115692-56-3 2,4-dibenzyloxyphenylacetic acid p-nitrophenyl ester 
• 151255-92-4 di-O-benzyl-penta-N-Boc-argiotoxin-636 
• 151255-93-5 penta-N-Boc-argiotoxin-636 

Relevant articles and documents

A MANUFACTURING PROCESS OF ISOFLAVAN OR ISOFLAVENE DERIVATIVES

The present invention relates to a method of synthesizing isoflavan and isoflavene derivatives of the Formula 1, which have the biological efficacy of antioxidation and protection against ultraviolet light. The method is effective and suitable for a mass production of isoflavan and isoflavene derivatives, which is a more convenient alternative preparation method compared to the isolation method by the extraction of plants, such as licorice, via troublesome preparative processes.

Synthesis and assay of hybrid analogs of argiotoxin-636 and philanthoxin-433: Glutamate receptor antagonists

The synthesis of the non-competitive glutamate receptor antagonist, argiotoxin-636 is described. Furthermore, synthetic routes are presented for the preparation of structural analogs including argiotoxin-philanthotoxin hybrids. Biological activities on gl