sales@angenesci.com
Login | Register
logo
Structures Search
Home Other Building Blocks 1,1,1,3,3,3-Hexafluoropropan-2-yl acrylate

1,1,1,3,3,3-Hexafluoropropan-2-yl acrylate

CAS No.:
2160-89-6
Catalog Number:
AG003D58
Molecular Formula:
Molecular Weight:
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25g
>98.0%(GC)
1 week
United States
$231
- +
Product Description
Catalog Number:
AG003D58
Chemical Name:
1,1,1,3,3,3-Hexafluoropropan-2-yl acrylate
CAS Number:
2160-89-6
MDL Number:
MFCD00040104
IUPAC Name:
1,1,1,3,3,3-hexafluoropropan-2-yl prop-2-enoate
InChI:
InChI=1S/C6H4F6O2/c1-2-3(13)14-4(5(7,8)9)6(10,11)12/h2,4H,1H2
InChI Key:
MNSWITGNWZSAMC-UHFFFAOYSA-N
EC Number:
218-479-1
Properties
Complexity:
214  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
222.012g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
222.086g/mol
Monoisotopic Mass:
222.012g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3  
Literature
Title Journal
Mechanical activation of catalysts for C-C bond forming and anionic polymerization reactions from a single macromolecular reagent. Journal of the American Chemical Society 20101124
Kinetic polymerization behavior of fluorinated monomers for dental use. Dental materials journal 20101001
Enantio- and stereoselective route to the phoslactomycin family of antibiotics: formal synthesis of (+)-fostriecin and (+)-phoslactomycin B. Chemical communications (Cambridge, England) 20091021
Beta-isocupreidine-catalyzed Baylis-Hillman reaction of chiral N-boc-alpha-amino aldehydes. Organic letters 20061109
beta-Isocupreidine-catalyzed asymmetric Baylis-Hillman reaction of imines. Organic letters 20030821
An enantio- and stereocontrolled synthesis of (-)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis-Hillman reaction. Chemical communications (Cambridge, England) 20011007
Properties