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Dicyclopropyl ketone

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Dicyclopropyl ketone Basic information

Product Name:
Dicyclopropyl ketone
Synonyms:
  • Dicyclopropyl ketone,95%
  • DICYCLOPROPYLMETHYLOXIME
  • DICYCLOPROPYL METHYL KETONE
  • Methanone,dicyclopropyl-
  • Dicyclopropyl Ketone, 97+%
  • DICYCLOPROPYLMETHANONE
  • DICYCLOPROPYL KETONE
  • CYCLOPROPYL KETONE
CAS:
1121-37-5
MF:
C7H10O
MW:
110.15
EINECS:
214-331-5
Product Categories:
  • C7 to C8
  • Carbonyl Compounds
  • Pharmaceutical Intermediates
  • Cyclopropanes
  • Simple 3-Membered Ring Compounds
  • Ketones
Mol File:
1121-37-5.mol
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Dicyclopropyl ketone Chemical Properties

Melting point:
44.0-44.5 °C
Boiling point:
160-162 °C(lit.)
Density 
0.977 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.467(lit.)
Flash point:
103 °F
storage temp. 
Store below +30°C.
Specific Gravity
0.957
Water Solubility 
Soluble in water.
BRN 
774172
InChI
InChI=1S/C7H10O/c8-7(5-1-2-5)6-3-4-6/h5-6H,1-4H2
InChIKey
BIPUHAHGLJKIPK-UHFFFAOYSA-N
SMILES
C(C1CC1)(C1CC1)=O
CAS DataBase Reference
1121-37-5(CAS DataBase Reference)
NIST Chemistry Reference
Methanone, dicyclopropyl-(1121-37-5)
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Safety Information

Hazard Codes 
F,Xn
Risk Statements 
10-36/37/38-20/21/22-5
Safety Statements 
16-36-26-3
RIDADR 
UN 1224 3/PG 3
WGK Germany 
3
Hazard Note 
Harmful/Flammable
HazardClass 
3
PackingGroup 
III
HS Code 
29142900

MSDS

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Dicyclopropyl ketone Usage And Synthesis

Chemical Properties

clear colourless to yellowish liquid

Uses

Dicyclopropyl Ketone is used as a reagent in the synthesis of a new class of potent and selective agonists of dimeric carbamoylguanidine-type histamine H2 receptor ligands. Also used in the preparation of chemical space analogs of PNU-282,987 and SSR180711, which have nicotinic receptor activity.

Preparation

Preparation of Dicyclopropyl ketone
Reaction: To a one liter three-necked flask fitted with a reflux condenser and a metal Hershberg stirrer there was added 600 ml. of 20% sodium hydroxide and 165g . (0.9mole) of 1,7 -dichloro-4-heptanone. The mixture was refluxed for 30 minutes with vigorous stirring, then steam distilled until the characteristic odor of dicyclopropyl ketone was absent from the distillate. The distillate was then saturated with potassium carbonate, the upper layer separated and the water layer extracted once with ether. The combined organic layers were dried over potassium carbonate. after removal of the ether there was dist illed 69g. (70%) of dicyclopropyl ketone, b.p . 69° at 20 mm, nD25 1.4648-1.4654.

References

[1] G A Olah, G Liang, G K Prakash. “The unusual Favorskii-Nazarov reaction of dicyclopropyl ketone.” Proceedings of the National Academy of Sciences of the United States of America (1976): 2945–6.
[2] Gerd Schrumpf, Thomas Alshuth. “Conformational equilibrium of dicyclopropyl ketone.” Spectrochimica acta. Part A: Molecular spectroscopy 43 7 (1987): Pages 939-942.

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