874130-59-3

Basic information

• Product Name: Propanoic acid, 2,2-dimethyl-, 3-acetyl-4-hydroxyphenyl ester
• CAS NO: 874130-59-3
• Molecular Formula: C13H16O4
• Molecular Weight: 236.268
• Mol File: 874130-59-3.mol

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 2,2-dimethyl-, 3-acetyl-4-hydroxyphenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 2,2-dimethyl-, 3-acetyl-4-hydroxyphenyl ester(874130-59-3)
• EPA Substance Registry System: Propanoic acid, 2,2-dimethyl-, 3-acetyl-4-hydroxyphenyl ester(874130-59-3)

Safety Data

• Hazardous Substances Data: 874130-59-3(Hazardous Substances Data)

Upstream product

• 3282-30-2 pivaloyl chloride 
• 490-78-8 2,5-Dihydroxyacetophenone 

Downstream Products

• 874130-67-3 2,2-dimethylpropionic acid 3-(2-(ethoxythiocarbonylsulfanyl)acetyl)-4-methoxyphenyl ester 
• 874130-60-6 2-iodo-3-methoxy-5-methylbenzoic acid 3-acetyl-4-methoxyphenyl ester 
• 31405-60-4 1-(5-hydroxy-2-methoxyphenyl)ethan-1-one 
• 874130-66-2 2,2-dimethylpropionic acid 3-acetyl-4-methoxyphenyl ester 
• 33857-20-4 1-(3-bromo-2,5-dihydroxy-phenyl)-ethanone 

Relevant articles and documents

Model studies towards the synthesis of gilvocarcin M

In model studies towards the synthesis of gilvocarcin M, a convergent, xanthate-based free-radical strategy was tested in order to construct the key aromatic ring attached to the sugar unit. The Royal Society of Chemistry 2005.

SUBSTITUTED BENZOHYDRAZIDE ANALOGS AS HISTONE DEMETHYLASE INHIBITORS

Benzohydrazide analogs, derivatives thereof, and related compounds, which are useful as inhibitors of lysine-specific histone demethyfase, including LSD1 and LSD2; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of using the compounds and compositions to treat disorders associated with dysfunction of the LSD1 and/or LSD2.

Activity-Based Proteome Profiling Probes Based on Woodward's Reagent K with Distinct Target Selectivity

Woodward's reagent K (WRK) is a reactive heterocyclic compound that has been employed in protein chemistry to covalently and unspecifically label proteins at nucleophilic amino acids, notably at histidine and cysteine. We have developed a panel of WRK-der