50882-16-1

Basic information

• Product Name: 2-CYCLOPENTANONE CARBOXYLATE
• Synonyms: 2-CYCLOPENTANONE CARBOXYLATE;2-OXOCYCLOPENTANECARBOXYLIC ACID;RARECHEM AL BO 1777;2-OXYCYCLOPENTANECARBOXYLIC ACID;CYCLOPENTANONE-2-CARBOXYLATE;2-Carboxycyclopentanone;2-Oxocyclopentane-1-carboxylic acid
• CAS NO: 50882-16-1
• Molecular Formula: C₆H₈O₃
• Molecular Weight: 128.13
• Mol File: 50882-16-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 301℃
• Flash Point: 150℃
• Appearance: /
• Density: 1.314
• Storage Temp.: -20°C Freezer
• Solubility: Chloroform, Methanol
• PKA: 3.60±0.20(Predicted)
• Stability: Temperature Sensitive
• CAS DataBase Reference: 2-CYCLOPENTANONE CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CYCLOPENTANONE CARBOXYLATE(50882-16-1)
• EPA Substance Registry System: 2-CYCLOPENTANONE CARBOXYLATE(50882-16-1)

Safety Data

• Hazardous Substances Data: 50882-16-1(Hazardous Substances Data)

Usage

Uses

2-Oxocyclopentanecarboxylic Acid is a reactant that has been used in the synthesis of Piragliatin, a glucokinase activator.

Upstream product

• 611-10-9 2-ethoxycarbonyl-1-cyclopentanone 
• 124-38-9 carbon dioxide 
• 120-92-3 cyclopentanone 
• 14171-36-9 methyl magnesium carbonate 
• 4861-79-4 magnesium methyl carbonate 
• 10472-24-9 methyl 2-oxocyclopentane-1-carboxylate 
• 98135-97-8 2-Hydroxy-cyclopenten-⁽¹⁾-carbonsaeure-⁽¹⁾ 
• 1460-08-8 2-diazocyclohexane-1,3-dione 

Downstream Products

• 23153-73-3 ethyl 1,4-dioxaspiro[4,4]nonane-6-carboxylate 
• 120-92-3 cyclopentanone 
• 142-29-0 cyclopentene 

Relevant articles and documents

Application of copper(II)-mediated radical cross-dehydrogenative coupling to prepare spirocyclic oxindoles and to a formal total synthesis of Satavaptan

Application of radical cross-dehydrogenative coupling (CDC) procedures to prepare a range of novel spirocyclic oxindoles and to a formal total synthesis of the vasopressin V2 receptor antagonist Satavaptan is reported. The key step involves a c

Synthesis of potent, substituted carbazoles as selective androgen receptor modulators (SARMs)

The synthesis and in vitro binding affinity for a novel series of potent androgen receptor modulators is described. One of the more potent compounds (17, RAD35010) was further characterized in vivo where it restored levator ani weight in castrated male ra

The 2-oxocyclopentanecarboxylic acid keto-enol system in aqueous solution: Generation of the enol by hydration of an acylketene

Flash photolysis of 2-diazocyclohexane-1,3-dione in aqueous solution produced 2-ketocyclopentylideneketene, which hydrated to the enol of 2-oxocyclopentanecarboxylic acid, and the enol then isomerized to the keto form of the acid. This ketene proved to be