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Cyclobutanemethanol

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Cyclobutanemethanol Basic information

Product Name:
Cyclobutanemethanol
Synonyms:
  • (HYDROXYMETHYL)CYCLOBUTANE
  • cyclobutylcarbinol
  • CYCLOBUTYLMETHANOL
  • CYCLOBUTANECARBINOL
  • CYCLOBUTANEMETHANOL
  • RARECHEM AK ML 0579
  • Cyclobutanemethanol,99%
  • Cyclobutylcarbinol~Hydroxymethylcyclobutane
CAS:
4415-82-1
MF:
C5H10O
MW:
86.13
EINECS:
224-575-4
Product Categories:
  • Benazir bhutto, Nadine brown brown, analgesic, such as intermediates.
  • API intermediates
  • Cyclobutanes & Cyclobutenes
  • Simple 4-Membered Ring Compounds
  • Cycloalkanes
  • Alcohols
  • C2 to C6
  • Oxygen Compounds
Mol File:
4415-82-1.mol
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Cyclobutanemethanol Chemical Properties

Melting point:
68.5 °C
Boiling point:
143-144 °C(lit.)
Density 
0.913 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.446(lit.)
Flash point:
104 °F
storage temp. 
Sealed in dry,2-8°C
pka
15.26±0.10(Predicted)
form 
Liquid
color 
Clear colorless
Water Solubility 
immiscible
BRN 
2036027
InChIKey
WPOPOPFNZYPKAV-UHFFFAOYSA-N
CAS DataBase Reference
4415-82-1(CAS DataBase Reference)
NIST Chemistry Reference
Cyclobutanemethanol(4415-82-1)
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Safety Information

Risk Statements 
10
Safety Statements 
16-24/25
RIDADR 
UN 1987 3/PG 3
WGK Germany 
3
HazardClass 
3
PackingGroup 
III
HS Code 
29061900

MSDS

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Cyclobutanemethanol Usage And Synthesis

Chemical Properties

Colorless to Almost colorless clear liquid.

Uses

Cyclobutanemethanol was used in the synthesis of bicyclic lactone.

Application

Cyclobutanemethanol is a drug used to treat inflammatory diseases. It is an uptake inhibitor that blocks the transport of uridine into cells, preventing the activation of G-protein coupled receptors and the subsequent production of inflammatory mediators. Cyclobutanemethanol has been shown to have anti-inflammatory properties by inhibiting the CB2 receptor, which is found in large quantities in inflammatory tissues. It also prevents dehydration and increases blood flow to inflamed areas by acting on vascular endothelial cells. It has been shown to inhibit influenza virus replication in vitro, but not in vivo.

General Description

Oxidation of cyclobutanemethanol in the presence of lead tetraacetate and lead tetraacetate/metal chloride has been investigated.

Synthesis

Cyclobutanemethanol can be synthesized from two molecules of hydrochloric acid and one molecule of cyclobutane. The synthesis pathway includes removal of a hydroxy group and addition of an alkynyl group via hydrogen bonding interactions with chloride ions.

Cyclobutanemethanol Preparation Products And Raw materials

Raw materials

Preparation Products

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