221021-36-9

Basic information

• Product Name: 3'-FORMYLBIPHENYL-4-CARBOXYLIC ACID METHYL ESTER
• Synonyms: 4-(3-FORMYLPHENYL)BENZOIC ACID METHYL ESTER;3'-FORMYLBIPHENYL-4-CARBOXYLIC ACID METHYL ESTER;AKOS BAR-0263;METHYL 4-(3-FORMYLPHENYL)BENZOATE;METHYL 3'-FORMYL[1,1'-BIPHENYL]-4-CARBOXYLATE;SALOR-INT L480606-1EA;4-(3-(Formylphenyl)phenylsulfonic acid;Methyl 4-(3-formylphenyl)benzoate 97%
• CAS NO: 221021-36-9
• Molecular Formula: C₁₅H₁₂O₃
• Molecular Weight: 240.25
• Mol File: 221021-36-9.mol

Chemical Properties

• Melting Point: 97-101 °C
• Boiling Point: 402.4 °C at 760 mmHg
• Flash Point: 180 °C
• Appearance: /
• Density: 1.176 g/cm³
• CAS DataBase Reference: 3'-FORMYLBIPHENYL-4-CARBOXYLIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-FORMYLBIPHENYL-4-CARBOXYLIC ACID METHYL ESTER(221021-36-9)
• EPA Substance Registry System: 3'-FORMYLBIPHENYL-4-CARBOXYLIC ACID METHYL ESTER(221021-36-9)

Safety Data

• Hazard Codes: N,Xi
• Statements: 50/53
• Safety Statements: 60-61
• RIDADR: UN 3077 9/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 221021-36-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3'-Formylbiphenyl-4-carboxylic acid methyl ester is used as a building block for the synthesis of new pharmaceutical compounds. Its unique chemical structure allows for the development of innovative drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 3'-Formylbiphenyl-4-carboxylic acid methyl ester is used as a precursor in the synthesis of various agrochemicals. Its versatility in chemical reactions enables the creation of new compounds with potential applications in crop protection and pest control.
Used in Organic Materials Research and Development:
3'-Formylbiphenyl-4-carboxylic acid methyl ester is utilized as a key component in the research and development of organic materials. Its unique properties contribute to the creation of novel materials with potential applications in various industries, such as electronics, coatings, and plastics.
Used in Chemical Synthesis:
3'-Formylbiphenyl-4-carboxylic acid methyl ester is used as a reagent in various chemical synthesis processes. Its ability to participate in a wide range of chemical reactions makes it a valuable tool for creating new organic compounds with diverse applications.

Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 222180-23-6 3’-formyl-[1,1’-biphenyl]-4-carboxylic acid 
• 74-88-4 methyl iodide 
• 99768-12-4 4-methoxycarbonylphenylboronic acid 

Downstream Products

• 223126-96-3 methyl 3'-(hydroxymethyl)biphenyl-4-carboxylate 
• 1311291-88-9 methyl 3'-(bromomethyl)biphenyl-4-carboxylate 
• 1311292-02-0 C₃₂H₃₆N₆O₆ 
• 222180-23-6 3’-formyl-[1,1’-biphenyl]-4-carboxylic acid 

Relevant articles and documents

HETEROCYCLIC INTEGRIN AGONISTS

The present invention provides polycyclic oxothioxoimidazolidines, dioxoimidazolines, oxothioxooxazolidines, dioxooxazolidines, and related compounds, which are useful as integrin agonists. Methods for the treatment of integrin-mediated diseases such as cancer are also described.

1H-INDOLE-2-CARBOXYLIC ACID DERIVATIVES USEFUL AS PPAR MODULATORS

The present invention relates to certain indole derivatives that are modulators of PPAR, to processes for their preparation, to pharmaceutical compositions containing them and to their use in medicine.

Amidocarboxylic acid derivatives

Amidocarboxylic acid derivatives of the formula: wherein R1 represents a hydrogen atom, etc.; R2 represents an alkylene group; R3 represents a hydrogen atom, etc.; R4 represents a hydrogen atom, etc.; X represents a substituted or unsubstituted aryl group, etc.,; Y represents an oxygen atom, etc.; Z represents an alkylene group, etc.; and W represents an alkyl group, etc.; and pharmacologically acceptable salts thereof and pharmacologically acceptable esters thereof are useful as the active ingredient of pharmaceutical compositions. They may be used to treat specified diseases, including diabetes mellitus, hyperlipemia, arteriosclerosis, hypertension, etc.

Palladium-catalyzed coupling of functionalized bromoarenes to a polystyrene-bound aryl tributylstannane

The Stille reaction with a polystyrene-bound stannyl component, catalyzed by a palladacycle complex, provides a convenient and clean method for the synthesis of substituted biaryls on the resin. Several functional groups useful for the construction of supported polydentate amino alcohols were successfully introduced.