1076-99-9

Usage

Uses

Used in Pharmaceutical Industry:
4-ALLYL-BENZOIC ACID is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 4-ALLYL-BENZOIC ACID is utilized as an intermediate in the production of agrochemicals, aiding in the creation of substances that protect crops and enhance agricultural productivity.
Used in Organic Compounds Synthesis:
4-ALLYL-BENZOIC ACID is employed as a key component in the synthesis of organic compounds, playing a crucial role in the formation of complex organic molecules for various applications.
Used in Polymer and Resin Production:
As a building block in polymer and resin manufacturing, 4-ALLYL-BENZOIC ACID is used to create materials with specific properties, such as durability and resistance, for use in a wide array of industries.
Used in Research and Development:
4-ALLYL-BENZOIC ACID is used as a subject of study for its potential anti-inflammatory and anticancer properties, with ongoing research aimed at exploring and harnessing these effects for medical applications.

InChI:InChI=1/C10H10O2/c1-2-3-8-4-6-9(7-5-8)10(11)12/h2,4-7H,1,3H2,(H,11,12)

Upstream product

• 1745-18-2 1-allyl-4-chlorobenzene 
• 124-38-9 carbon dioxide 
• 106-95-6 allyl bromide 
• 19819-94-4 4-allyl-benzoic acid ethyl ester 
• 619-58-9 4-iodobenzoic acid 
• 51934-41-9 4-iodobenzoic acid ethyl ester 
• 106-46-7 para-dichlorobenzene 
• 150-13-0 4-amino-benzoic acid 
• 762-72-1 allyl-trimethyl-silane 
• 15719-64-9 methylammonium carbonate 

Downstream Products

• 808748-89-2 2-p-allylbenzoyl-2'-O-tert-butyldimethylsilyl-3'-de-tert-butoxycarbonyl-3'-heptenoyl-7,10-ditriethylsilyldocetaxel 

Relevant academic research and scientific papers

Cross-Coupling Reactions of Aryldiazonium Salts with Allylsilanes under Merged Gold/Visible-Light Photoredox Catalysis

A method for the cross-coupling reactions of aryldiazonium salts with trialkylallylsilanes via merged gold/photoredox catalysis is described. The reaction is proposed to proceed through a photoredox-promoted generation of an electrophilic arylgold(III) intermediate that undergoes transmetalation with allyltrimethylsilane to form allylarenes.

Method for producing Grignard compounds

The invention relates to a process for preparing Grignard compounds of the formula I. The invention additionally relates to compounds of the formula I and to polymer-bound compounds of the formula Ia. The invention further relates to the use of the process for preparing substance libraries and to the use of the compounds of the formulae I and Ia in chemical synthesis.

Synthesis of C2-C3′N-linked macrocyclic taxoids. Novel docetaxel analogues with high tubulin activity

Novel C2-C3′N-linked macrocyclic taxoids 4 bearing an aromatic ring at position C2 were synthesized. These compounds, tethered between N3′ and the C2-aromatic ring at the ortho, meta, or para position, were constructed by ring-closing metathesis. The para

Preparation of highly functionalized Grignard reagents by an iodine-magnesium exchange reaction and its application in solid-phase synthesis

At -40°C aryl iodides that contain other functional groups can be selectively converted into Grignard reagents, which react with electrophiles such as benzaldehyde in the usual manner [Eq. (a)]. Aryl bromides and iodides that are immobilized as esters on a Wang resin behave analogously.

Cyclic Siloxanes with Mesogenic Side Groups

Cyclic liquid crystalline siloxanes (CLCS) are optical uniaxial positive (SA, N) and negative (N*) materials in accordance with calamitic structures.X-Ray measurements indicate, that the distances of SA layers correspond with the length of the monomer unit.In the case of mesogens with high polarity the distance is 1.7 fold the length of the monomer unit.A bundle model is proposed for CLC siloxanes.