Home Aldehydes Cyclopropanecarboxaldehyde

Cyclopropanecarboxaldehyde

CAS No.:
1489-69-6
Catalog Number:
AG001LAD
Molecular Formula:
C4H6O
Molecular Weight:
70.0898
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$32
- +
25g
98%
In Stock USA
United States
$88
- +
100g
98%
In Stock USA
United States
$257
- +
500g
98%
In Stock USA
United States
$898
- +
Product Description
Catalog Number:
AG001LAD
Chemical Name:
Cyclopropanecarboxaldehyde
CAS Number:
1489-69-6
Molecular Formula:
C4H6O
Molecular Weight:
70.0898
MDL Number:
MFCD00012261
IUPAC Name:
cyclopropanecarbaldehyde
InChI:
InChI=1S/C4H6O/c5-3-4-1-2-4/h3-4H,1-2H2
InChI Key:
JMYVMOUINOAAPA-UHFFFAOYSA-N
SMILES:
O=CC1CC1
Properties
Complexity:
45.6  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
70.042g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
70.091g/mol
Monoisotopic Mass:
70.042g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2  
Literature
Title Journal
Cyclopropylhydroxycarbene. Journal of the American Chemical Society 20110831
Steric effects on the enantiodiscrimination of diproline chiral stationary phases in the resolution of racemic compounds. Journal of chromatography. A 20110812
Stereoselective routes to aryl substituted γ-butyrolactones and their application towards the synthesis of highly oxidised furanocembranoids. Organic & biomolecular chemistry 20110507
Cyclopropane-aldehyde annulations at quaternary donor sites: stereoselective access to highly substituted tetrahydrofurans. Organic letters 20110415
Chemo-, regio-, and diastereoselectivity preferences in the reaction of a sulfur ylide with a dienal and an enone. Organic & biomolecular chemistry 20110307
Complexity-building annulations of strained cycloalkanes and C═O π bonds. The Journal of organic chemistry 20101001
Synthesis and antiproliferative activity of indolizine derivatives incorporating a cyclopropylcarbonyl group against Hep-G2 cancer cell line. European journal of medicinal chemistry 20100701
N-heterocyclic carbene-catalyzed domino ring-opening/redox amidation/cyclization reactions of formylcyclopropane 1,1-diesters: direct construction of a 6-5-6 tricyclic hydropyrido[1,2-a]indole skeleton. The Journal of organic chemistry 20090605
Reactions of monoaryl-substituted methylenecyclobutanes and methylenecyclopropanes with 1-hydroxybenzotriazole (HOBt), 1-hydroxy-7-azabenzotriazole (HOAt), and 1-hydroxysuccinimide (HOSu). The Journal of organic chemistry 20090320
Action of N-acylated ambroxol derivatives on secretion of chloride ions in human airway epithelia. Biochemical and biophysical research communications 20090313
Measuring picosecond isomerization kinetics via broadband microwave spectroscopy. Science (New York, N.Y.) 20080516
One-pot organocatalytic domino Michael/alpha-alkylation reactions: direct catalytic enantioselective cyclopropanation and cyclopentanation reactions. Chemistry (Weinheim an der Bergstrasse, Germany) 20080101
Cyclopropylmethyl/cyclobutyl rearrangements on surfaces: evidence for transient cation formation near O-covered Mo(110). Journal of the American Chemical Society 20070418
Cyclopropanation of enantiopure metal alkenyl carbenes with 2-methoxyfuran: a practical route to carboxycyclopropylglycine precursors. Chemistry (Weinheim an der Bergstrasse, Germany) 20070101
Enzyme inhibition potency enhancement by active site metal chelating and hydrogen bonding induced conformation-restricted cyclopropanecarbonyl derivatives. Bioorganic & medicinal chemistry letters 20061201
Asymmetric halo-Mannich-type reaction provides access to pyrrolidines and beta-proline derivatives. The Journal of organic chemistry 20050916
Atmospheric chemistry of C3-C6 cycloalkanecarbaldehydes. The journal of physical chemistry. A 20050616
New asymmetric halo aldol reaction provides a novel approach to biologically important chiral cyclothers and cycloamines. Organic letters 20040610
Properties