Basic information Safety Supplier Related

3-Oxocyclopentanecarboxylic acid

Basic information Safety Supplier Related

3-Oxocyclopentanecarboxylic acid Basic information

Product Name:
3-Oxocyclopentanecarboxylic acid
Synonyms:
  • 3-OXOCYCLOPENTANE-1-CARBOXYLIC ACID
  • 3-OXOCYCLOPENTANECARBOXYLIC ACID
  • 3-OXO-1-CYCLOPENTANECARBOXYLIC ACID
  • [(4-Methyl-2-pyrimidinyl)sulfanyl]acetic acid
  • 3-ketocyclopentanecarboxylic acid
  • 3-Oxocyclopentanecar
  • 1-Carboxy-3-oxocyclopentane
  • 3-Oxocyclopentanecarboxyl...
CAS:
98-78-2
MF:
C6H8O3
MW:
128.13
Product Categories:
  • pharmacetical
  • Carbonyl Compounds
  • Carboxylic Acids
  • C6
Mol File:
98-78-2.mol
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3-Oxocyclopentanecarboxylic acid Chemical Properties

Melting point:
59-62 °C (lit.)
Boiling point:
150°C/1.5mmHg(lit.)
Density 
1.314±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
pka
4.62±0.20(Predicted)
color 
White to Almost white
InChI
InChI=1S/C6H8O3/c7-5-2-1-4(3-5)6(8)9/h4H,1-3H2,(H,8,9)
InChIKey
RDSNBKRWKBMPOP-UHFFFAOYSA-N
SMILES
C1(C(O)=O)CCC(=O)C1
CAS DataBase Reference
98-78-2(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39
WGK Germany 
3
HS Code 
29183000

MSDS

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3-Oxocyclopentanecarboxylic acid Usage And Synthesis

Chemical Properties

White powder

Uses

3-Oxo-1-cyclopentanecarboxylic acid is a useful chemical reagent.

Uses

3-Oxo-1-cyclopentanecarboxylic acid may be used in the preparation of 3-hydroxycyclopentanecarboxylic acid via hydrogenation.

Definition

ChEBI: 3-oxocyclopentanecarboxylic acid is an alicyclic ketone that is oxocyclopentanone substituted at position 3 by a carboxy group. It is a 4-oxo monocarboxylic acid and an alicyclic ketone. It is a conjugate acid of a 3-oxocyclopentanecarboxylate.

General Description

3-Oxo-1-cyclopentanecarboxylic acid , also known as 3-oxocyclopentanecarboxylic acid, is a keto acid derivative. It undergoes Curtius rearrangement with diphenyl phosphoryl azide and triethylamine in tert-butanol to form the corresponding boc-protected 1-(3-oxo)urea derivative.

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