- Bromodifluoroacetyl chloride
chembox new
ImageFile = Bromodifluoroacetylchloride.png
ImageSize = 250px
IUPACName = 2-bromo-2,2-difluoro-ethanoyl chloride
OtherNames =
Section1 = Chembox Identifiers
Abbreviations =
CASNo = 3832-48-2
EINECS =
PubChem = 520892
SMILES = C(=O)(C(F)(F)Br)Cl
InChI =
RTECS =
MeSHName =
ChEBI =
KEGG =
ATCCode_prefix =
ATCCode_suffix =
ATC_Supplemental =
Section2 = Chembox Properties
C = 2 | O = 1 | F = 2 | Br = 1 | Cl = 1
Appearance = liquid
Density =
MeltingPt =
Melting_notes =
BoilingPt = 50°C
Boiling_notes =
Solubility =
SolubleOther =
Solvent =
pKa =
pKb =
IsoelectricPt =
LambdaMax =
Absorbance =
SpecRotation =
RefractIndex =
Viscosity =
Dipole =
Section3 = Chembox Structure
CrystalStruct =
Coordination =
MolShape =
Section4 = Chembox Thermochemistry
DeltaHf =
DeltaHc =
Entropy =
HeatCapacity =
Section5 = Chembox Pharmacology
AdminRoutes =
Bioavail =
Metabolism =
HalfLife =
ProteinBound =
Excretion =
Legal_status =
Legal_US =
Legal_UK =
Legal_AU =
Legal_CA =
PregCat =
PregCat_AU =
PregCat_US =
Section6 = Chembox Explosive
ShockSens =
FrictionSens =
ExplosiveV =
REFactor =
Section7 = Chembox Hazards
ExternalMSDS = [http://www.apolloscientific.co.uk/downloads/msds/PC6436_msds.pdf]
EUClass = Corrosive (C)
EUIndex =
MainHazards =
NFPA-H =
NFPA-F =
NFPA-R =
NFPA-O =
RPhrases = R34
SPhrases = S36/37/39, S45
RSPhrases =
FlashPt =
Autoignition =
ExploLimits =
PEL =
Section8 = Chembox Related
OtherAnions =
OtherCations =
OtherFunctn =
Function =
OtherCpds =Bromodifluoroacetyl chloride is a
chemical compound with the formula BrCF2COCl. It has been used as a starting material for the synthesis of (biologically active) α,α-difluoro-γ-lactams [cite journal | author = Hideo Nagashima, Yoshimi Isono, and Sho-ichi Iwamatsu | title = Copper-Catalyzed Cyclization of N-Allylhalodifluoroacetamides: An Efficient Synthesis of α,α-difluoro-γ-lactams | journal =J. Org. Chem. | volume = 66 | issue = 1 | pages = 315-319 | year = 2001 | doi = 10.1021/jo001187f] and has been used in the synthesis of trifluoromethylated C-nucleoside s [cite journal | author = Constantin Mamata, Martin Heina and Ralf Miethchen | title = Fluorinated acyclo-C-nucleoside analogues from glycals in two steps | journal =Carbohydr. Res. | volume = 341 | issue = 10 | pages = 1758-1763 | year = 2006 | doi = 10.1016/j.carres.2006.01.011]References
ee also
*
Acetyl chloride
*Trifluoroacetic acid
Wikimedia Foundation. 2010.