Cyclobutanecarboxylic acid
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.020.975
EC Number
  • 223-072-7
UNII
  • InChI=1S/C5H8O2/c6-5(7)4-2-1-3-4/h4H,1-3H2,(H,6,7)
    Key: TXWOGHSRPAYOML-UHFFFAOYSA-N
  • C1CC(C1)C(=O)O
Properties
C5H8O2
Molar mass 100.117 g·mol−1
Appearance colorless liquid
Melting point −7.5 °C (18.5 °F; 265.6 K)
Boiling point 191.5–193.5 °C (376.7–380.3 °F; 464.6–466.6 K) 740 mm
Hazards
GHS labelling:[1]
GHS05: CorrosiveGHS07: Exclamation mark
Danger
H302, H312, H314, H332
P260, P261, P264, P270, P271, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P330, P362+P364, P363, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Cyclobutanecarboxylic acid is the organic compound with the formula C4H7CO2H. It is a colorless nonvolatile liquid. It can be prepared by decarboxylation of 1,1-cyclobutanedicarboxylic acid.[2] Cyclobutanecarboxylic acid is an intermediate in organic synthesis. For example, it is a precursor to cyclobutylamine.[3]

References

  1. ↑ "Cyclobutanecarboxylic acid". pubchem.ncbi.nlm.nih.gov.
  2. ↑ "1,1-Cyclobutanedicarboxylic Acid and Cyclobutanecarboxylic Acid". Organic Syntheses. 23: 16. 1943. doi:10.15227/orgsyn.023.0016.
  3. ↑ Newton W. Werner, Joseph Casanova, Jr. (1967). "Cyclobutylamine". Organic Syntheses. 47: 28. doi:10.15227/orgsyn.047.0028.{{cite journal}}: CS1 maint: multiple names: authors list (link)
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.