Substance
ID:344454
Names and Identifiers
Synonyms
Bromotripyrrolidinophosphonium hexafluorophosphate三吡咯烷基溴化鏻六氟磷酸盐PyBroP®
IUPAC name
bromotris(pyrrolidin-1-yl)phosphanium; hexafluoro-λ5-phosphanuide
IUPAC Traditional name
bromotris(pyrrolidin-1-yl)phosphanium hexafluorophosphate
Registration numbers
CAS Number
MDL Number
Beilstein Number
PubChem SID
Properties
Product Information
Purity
≥95.0% (HPLC)
Empirical Formula (Hill Notation)
C12H24BrF6N3P2
Safety Information
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
GHS Hazard statements
H314
German water hazard class
3
European Hazard Symbols
Corrosive (C)Risk Statements
34
MSDS Link
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Storage Temperature
-20°C
GHS Precautionary statements
P280-P305+P351+P338-P310
Safety Statements
26-27-36/37/39-45
GHS Signal Word
Danger
Molecule Details
Other Notes
Reactive peptide coupling reagent suitable for α,α-dialkyl amino acids5; Synthesis of depsipeptides6
Packaging
1 g in poly tube
5, 25 g in poly bottle
Application
Catalyst for: Synthesis of primary amides1 Direct dehydrative phosphonium cross coupling2 Direct arylation3 Pyrrolidide formation by phosphonium salt coupling reagents4
Legal Information
PyBroP is a registered trademark of Merck KGaA
Reactive peptide coupling reagent suitable for α,α-dialkyl amino acids5; Synthesis of depsipeptides6
Packaging
1 g in poly tube
5, 25 g in poly bottle
Application
Catalyst for: Synthesis of primary amides1 Direct dehydrative phosphonium cross coupling2 Direct arylation3 Pyrrolidide formation by phosphonium salt coupling reagents4
Legal Information
PyBroP is a registered trademark of Merck KGaA
Molecular Spectra
No Data Available
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References
No Data Available
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