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720-73-0

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720-73-0 Usage

Description

4'-METHYLBIPHENYL-4-CARBOXYLIC ACID is an organic compound characterized by the presence of COOH and CH groups in its molecular structure. It is known for its unique absorption bands and can undergo successive oxidation states, including alcohol, aldehyde, and carboxylic acids.

Uses

Used in Chemical Analysis:
4'-METHYLBIPHENYL-4-CARBOXYLIC ACID is used as a chemical compound for photoproduct analysis. It is analyzed using techniques such as GC-MS, ETIR, and GC-FTIR to confirm the three successive oxidation states of methyl substituents.
Used in Organic Chemistry Research:
4'-METHYLBIPHENYL-4-CARBOXYLIC ACID is used as a research compound in the field of organic chemistry. Its unique properties and oxidation states make it a valuable subject for studying chemical reactions and mechanisms.
Used in Pharmaceutical Industry:
4'-METHYLBIPHENYL-4-CARBOXYLIC ACID can be used as a building block or intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties can contribute to the development of new drugs and therapies.
Used in Material Science:
4'-METHYLBIPHENYL-4-CARBOXYLIC ACID can be used in the development of new materials with specific properties. Its ability to undergo oxidation states can be utilized in creating materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 720-73-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 720-73:
(5*7)+(4*2)+(3*0)+(2*7)+(1*3)=60
60 % 10 = 0
So 720-73-0 is a valid CAS Registry Number.

720-73-0 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H34459)  4'-Methylbiphenyl-4-carboxylic acid, 96%   

  • 720-73-0

  • 1g

  • 432.0CNY

  • Detail
  • Alfa Aesar

  • (H34459)  4'-Methylbiphenyl-4-carboxylic acid, 96%   

  • 720-73-0

  • 5g

  • 1833.0CNY

  • Detail

720-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methylphenyl)benzoic acid

1.2 Other means of identification

Product number -
Other names [1,1‘-Biphenyl]-4-carboxylic acid, 4‘-methyl-

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:720-73-0 SDS

720-73-0Relevant articles and documents

Preparation of metal-immobilized methacrylate-based monolithic columns for flow-through cross-coupling reactions

Sabarudin, Akhmad,Shu, Shin,Umemura, Tomonari,Yamamoto, Kazuhiro

, (2021/12/17)

With the aim of developing efficient flow-through microreactors for high-throughput organic synthesis, in this work, microreactors were fabricated by chemically immobilizing palladium-, nickel-, iron-, and copper-based catalysts onto ligand-modified poly(glycidyl methacrylate-co-ethylene dimethacrylate) [poly(GMA-co-EDMA)] monoliths, which were prepared inside a silicosteel tubing (10 cm long with an inner diameter of 1.0 mm) and modified with several ligands including 5-amino-1,10-phenanthroline (APHEN), iminodiacetic acid (IDA), and iminodimethyl phosphonic acid (IDP). The performance of the resulting microreactors in Suzuki?Miyaura cross-coupling reactions was evaluated, finding that the poly(GMA-co-EDMA) monolith chemically modified with 5-amino-1,10-phenanthroline as a binding site for the palladium catalyst provided an excellent flow-through performance, enabling highly efficient and rapid reactions with high product yields. Moreover, this monolithic microreactor maintained its good activity and efficiency during prolonged use.

N-Acylsulfonamide apoptosis promoters

-

, (2008/06/13)

N-Benzoyl arylsulfonamides having the formula Are BCL-X1 inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-X1 inhibiting compositions and methods of promoting apoptosis in a mammal.

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