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Home Other Building Blocks Cyclopropyl methyl ketone

Cyclopropyl methyl ketone

CAS No.:
765-43-5
Catalog Number:
AG0032R2
Molecular Formula:
C5H8O
Molecular Weight:
84.1164
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
96%
In Stock USA
United States
$13
- +
25g
96%
In Stock USA
United States
$19
- +
100g
96%
In Stock USA
United States
$63
- +
500g
96%
In Stock USA
United States
$250
- +
Product Description
Catalog Number:
AG0032R2
Chemical Name:
Cyclopropyl methyl ketone
CAS Number:
765-43-5
Molecular Formula:
C5H8O
Molecular Weight:
84.1164
MDL Number:
MFCD00001297
IUPAC Name:
1-cyclopropylethanone
InChI:
InChI=1S/C5H8O/c1-4(6)5-2-3-5/h5H,2-3H2,1H3
InChI Key:
HVCFCNAITDHQFX-UHFFFAOYSA-N
SMILES:
CC(=O)C1CC1
EC Number:
212-146-4
UNII:
N27YY1XCFH
NSC Number:
1940
Properties
Complexity:
72  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
84.058g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
84.118g/mol
Monoisotopic Mass:
84.058g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  
Literature
Title Journal
Male-produced sex pheromone of the stink bug Edessa meditabunda. Journal of chemical ecology 20120701
Preparation and evaluation of 5, 9-dimethyl-2-cyclopropyl-2-decanol as a penetration enhancer for drugs through rat skin. Pakistan journal of pharmaceutical sciences 20111001
Synthesis and reactivity of six-membered oxa-nickelacycles: a ring-opening reaction of cyclopropyl ketones. Chemistry (Weinheim an der Bergstrasse, Germany) 20091005
(Z)- and (E)-2-(1,2-dihydroxyethyl)methylenecyclopropane analogues of 2'-deoxyadenosine and 2'-deoxyguanosine. Synthesis of all stereoisomers, absolute configuration, and antiviral activity. Journal of medicinal chemistry 20090528
Synthesis of spiropyrans: H-abstractions in 3-cycloalkenyloxybenzopyrans. Beilstein journal of organic chemistry 20070101
Synthesis of 1,2,4-trioxepanes and 1,2,4-trioxocanes via photooxygenation of homoallylic alcohols. The Journal of organic chemistry 20061124
Designing the 'search pathway' in the development of a new class of highly efficient stereoselective hydrosilylation catalysts. Chemistry (Weinheim an der Bergstrasse, Germany) 20050422
Properties