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2-[2-(4-Methoxyphenyl)ethyl]benzoic Acid, also known as a Dibenzocycloheptene precursor, is an off-white solid with unique chemical properties. It is a complex organic molecule derived from benzoic acid, featuring a methoxyphenylethyl group attached to its structure. 2-[2-(4-METHOXYPHENYL)ETHYL]BENZOIC ACID is known for its role in the synthesis of Dibenzocycloheptenes, which are important in various chemical and pharmaceutical applications.

14525-71-4

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14525-71-4 Usage

Uses

Used in Pharmaceutical Industry:
2-[2-(4-Methoxyphenyl)ethyl]benzoic Acid is used as a reagent for the preparation of Dibenzocycloheptenes, which are significant in the development of pharmaceutical compounds. These Dibenzocycloheptenes have potential applications in the treatment of various medical conditions due to their unique chemical structures and properties.
Used in Chemical Synthesis:
In the chemical industry, 2-[2-(4-Methoxyphenyl)ethyl]benzoic Acid serves as a key intermediate in the synthesis of various organic compounds, including Dibenzocycloheptenes. These compounds are valuable for their diverse applications, such as in the development of new materials, catalysts, and other specialty chemicals.
Used in Research and Development:
2-[2-(4-Methoxyphenyl)ethyl]benzoic Acid is also utilized in research and development settings, where it contributes to the advancement of scientific knowledge and the discovery of new chemical reactions and processes. Its unique structure and properties make it an interesting subject for study, potentially leading to the development of novel applications and uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 14525-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,2 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14525-71:
(7*1)+(6*4)+(5*5)+(4*2)+(3*5)+(2*7)+(1*1)=94
94 % 10 = 4
So 14525-71-4 is a valid CAS Registry Number.

14525-71-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(4-Methoxyphenyl)ethyl]benzoic acid

1.2 Other means of identification

Product number -
Other names 4'-methoxy-bibenzyl-2-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14525-71-4 SDS

14525-71-4Relevant academic research and scientific papers

DIBENZOCYCLOHEPTENE COMPOUND

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Page 111, (2010/11/30)

The present invention discloses a dibenzocycloheptene compound represented by the formula (I): ???wherein R1: hydrogen atom, halogen atom, etc., R2: hydrogen atom, halogen atom, etc., A: 5-membered or 6-membered heteroaromatic ring group containing 1 to 3 hetero atom(s) selected from the group consisting of nitrogen atom, oxygen atom and sulfur atom, and the heteroaromatic ring group, etc. may have halogen atom, nitrogen atom, etc. as substituent(s), B: formula; -CH=CH-, formula; -CH2O-, etc., Y: C1-C10 alkylene group which may have halogen atom, etc. as substituent(s), etc., Z: carboxyl group which may be protected, etc., m: an integer of 1 to 4, n: an integer of 1 to 3, ???------ represents a single bond or a double bond, or a pharmaceutically acceptable salt thereof and a medical composition containing the same as an effective ingredient which has leukotriene C4 antagonistic action and leukotriene E4 antagonistic action in addition to potent leukotriene D4 antagonistic action, and useful as antiasthmatic agent, antiallergic agent and anti-inflammatory agent.

Convenient syntheses of 3-aryl-3,4-dihydroisocoumarins and lunularic acid derivatives

Mali, Raghao S.,Shelke, Dattatray W.

, p. 822 - 825 (2007/10/02)

A convenient two-step approach for the syntheses of 3-aryl-3,4-dihydroisocoumarins (13-17) including some naturally occurring 3-aryl-8-hydroxy-3,4-dihydroisocoumarins (1,2) and lunularic acid derivatives (18-21) is described from 2-formylbenzoic acids (4,

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