131524-43-1

Basic information

• Product Name: Benzoic acid, 2-formyl-3-hydroxy-, methyl ester
• CAS NO: 131524-43-1
• Molecular Formula: C9H8O4
• Molecular Weight: 180.16
• Mol File: 131524-43-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-formyl-3-hydroxy-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-formyl-3-hydroxy-, methyl ester(131524-43-1)
• EPA Substance Registry System: Benzoic acid, 2-formyl-3-hydroxy-, methyl ester(131524-43-1)

Safety Data

• Hazardous Substances Data: 131524-43-1(Hazardous Substances Data)

Usage

General Description

Benzoic acid, 2-formyl-3-hydroxy-, methyl ester is a chemical compound with the molecular formula C9H8O4. It is commonly known as 2-formyl-3-hydroxybenzoic acid methyl ester. This chemical is commonly used in the synthesis of various pharmaceuticals and natural products. It has also been studied for its potential use in the development of new drugs and treatments. Additionally, it has been used as a flavoring agent in food and beverages. Benzoic acid, 2-formyl-3-hydroxy-, methyl ester may have potential applications in various fields such as medicine, food science, and chemistry.

Upstream product

• 100-97-0 hexamethylenetetramine 
• 19438-10-9 methyl 3-hydroxybenzoate 
• 76-05-1 trifluoroacetic acid 

Downstream Products

• 1354349-00-0 methyl 2-benzoylbenzofuran-4-carboxylate 
• 1061604-41-8 3-(4-hydroxy-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione 
• 13161-32-5 4-hydroxy-3H-isobenzofuran-1-one 
• 2211-83-8 4-methyl-3H-isobenzofuran-1-one 
• 1021499-87-5 methyl 2-(2-ethoxycarbonylvinyl)-3-hydroxybenzoate 
• 609805-83-6 methyl 2-hydroxyiminomethyl-3-hydroxybenzoate 
• 151299-70-6 methyl 3-<(tert-butyldimethylsilyl)oxy>-2-dimethoxymethylbenzoate 
• 151299-72-8 3-<(tert-butyldimethylsilyl)oxy>-2-dimethoxymethylbenzyl formate 
• 151299-71-7 3-<(tert-butyldimethylsilyl)oxy>-2-dimethoxymethylbenzyl alcohol 
• 386708-35-6 2-dimethoxymethyl-3-hydroxymethylphenol 
• 386708-36-7 2-dimethoxymethyl-3-hydroxybenzenecarbaldehyde 
• 151299-69-3 methyl 2-dimethoxymethyl-3-hydroxybenzoate 
• 131524-42-0 hexyl rhizoglyphinate 

Relevant articles and documents

Total synthesis of neo-tanshinlactones through a cascade benzannulation-lactonization as the key step

The cascade annulation-lactonization of phthalides with α-carboxyfurylacrylates in the presence of lithium hexamethyldisilazide (LiHMDS) provides both convergent and semiconvergent regioselective syntheses of neo-tanshinlactones in moderate yields. This methodology also offers an avenue for the direct syntheses of hitherto unreported 6-alkoxycarbonyl-substituted neo-tanshinlactones and their heterocyclic analogues. A new synthesis of 4-alkyl phthalides was developed on the basis of a combination of a Duff reaction and Fuerstner cross-coupling. The cascade benzannulation-lactonization of phthalides with α-carboxyfurylacrylates was employed as the key reaction for the concise synthesis of neo-tanshinlactone. Copyright

PROCESSES FOR PREPARATION OF (S)-TERT-BUTYL 4,5-DIAMINO-5-OXOPENTANOATE

Provided are processes for the preparation of (S)-tert-butyl 4,5-diamino-5-oxopentanoate, or a salt, solvate, hydrate, enantiomer, mixture of enantiomers, or isotopologue thereof. Also provided are solid forms of various intermediates and products obtained from the processes.

A microwave-assisted domino rearrangement of propargyl vinyl ethers to multifunctionalized aromatic platforms

H makes a difference! A novel reactivity profile of propargyl vinyl ethers has been developed, which is controlled by the presence of a hydrogen atom at the homopropargylic position (see scheme; EWG=electron-withdrawing group). This strategy was conveniently used to construct multifunctionalized phenolic platforms, including salicylaldehydes and the corresponding ketone derivatives. Copyright