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Home Other Building Blocks Ethyl Bromodifluoroacetate

Ethyl Bromodifluoroacetate

CAS No.:
667-27-6
Catalog Number:
AG0034VW
Molecular Formula:
C4H5BrF2O2
Molecular Weight:
202.9821
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$8
- +
25g
95%
In Stock USA
United States
$15
- +
100g
95%
In Stock USA
United States
$43
- +
Product Description
Catalog Number:
AG0034VW
Chemical Name:
Ethyl Bromodifluoroacetate
CAS Number:
667-27-6
Molecular Formula:
C4H5BrF2O2
Molecular Weight:
202.9821
MDL Number:
MFCD00042069
IUPAC Name:
ethyl 2-bromo-2,2-difluoroacetate
InChI:
InChI=1S/C4H5BrF2O2/c1-2-9-3(8)4(5,6)7/h2H2,1H3
InChI Key:
IRSJDVYTJUCXRV-UHFFFAOYSA-N
SMILES:
CCOC(=O)C(Br)(F)F
EC Number:
211-567-0
Properties
Complexity:
115  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
201.944g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
202.983g/mol
Monoisotopic Mass:
201.944g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.6  
Literature
Title Journal
Synthesis of 4-substituted 3,3-difluoropiperidines. The Journal of organic chemistry 20100205
Addition of difluoromethyl radicals to glycals: a new route to alpha-CF2-D-glycosides. Organic letters 20070621
Stereocontrolled synthesis of beta-difluoromethylated materials. The Journal of organic chemistry 20050722
Convenient asymmetric synthesis of beta-substituted alpha,alpha-difluoro-beta-amino acids via Reformatsky reaction between Davis' N-sulfinylimines and ethyl bromodifluoroacetate. The Journal of organic chemistry 20030919
Asymmetric synthesis of alpha,alpha-difluoro-beta-amino acid derivatives from enantiomerically pure N-tert-butylsulfinimines. The Journal of organic chemistry 20021115
Properties