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Allyl methyl carbonate

CAS No.:
35466-83-2
Catalog Number:
AG0034FX
Molecular Formula:
C5H8O3
Molecular Weight:
116.1152
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
$100
- +
100g
98%
In Stock USA
United States
$319
- +
Product Description
Catalog Number:
AG0034FX
Chemical Name:
Allyl methyl carbonate
CAS Number:
35466-83-2
Molecular Formula:
C5H8O3
Molecular Weight:
116.1152
MDL Number:
MFCD00134545
IUPAC Name:
methyl prop-2-enyl carbonate
InChI:
InChI=1S/C5H8O3/c1-3-4-8-5(6)7-2/h3H,1,4H2,2H3
InChI Key:
YHLVIDQQTOMBGN-UHFFFAOYSA-N
SMILES:
COC(=O)OCC=C
EC Number:
468-750-5
Properties
Complexity:
87.7  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
116.047g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
116.116g/mol
Monoisotopic Mass:
116.047g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
35.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2  
Literature
Title Journal
Palladium(0)-catalyzed stereoselective cyclization of allenenes: divergent synthesis of pyrrolidines and 3-azabicyclo[3.1.0]hexanes from single allenenes. The Journal of organic chemistry 20040625
Tetrazole synthesis via the palladium-catalyzed three component coupling reaction. Molecular diversity 20030101
Palladium-catalyzed selective synthesis of 2-allyltetrazoles. The Journal of organic chemistry 20021018
Synthesis of allyl cyanamides and N-cyanoindoles via the palladium-catalyzed three-component coupling reaction. Journal of the American Chemical Society 20021009
Properties