Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
C9H16N2Cl · PF6
CAS Number:
Molecular Weight:
332.65
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
7898575
Quality Level
assay
≥97.5% (CHN)
form
solid
reaction suitability
reaction type: Coupling Reactions
mp
153-156 °C
application(s)
peptide synthesis
functional group
chloro
storage temp.
2-8°C
SMILES string
F[P-](F)(F)(F)(F)F.Cl\C(N1CCCC1)=[N+]2/CCCC2
InChI
1S/C9H16ClN2.F6P/c10-9(11-5-1-2-6-11)12-7-3-4-8-12;1-7(2,3,4,5)6/h1-8H2;/q+1;-1
InChI key
NHEGCUSBUWGOQM-UHFFFAOYSA-N
Application
Reactant for:
Enantioselective desymmetrization of meso-asiridines
Peptide coupling
Reagent for:
Heterocyclization of chloroformamidinium salts
Oxidative insertion for palladium and nickel catalyst synthesis
Enantioselective desymmetrization of meso-asiridines
Peptide coupling
Reagent for:
Heterocyclization of chloroformamidinium salts
Oxidative insertion for palladium and nickel catalyst synthesis
Other Notes
Crystalline and non-hygroscopic peptide coupling reagent, especially for N-methyl amino acids
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
Fluoroamidinium salts advance acid halogenation with greater stability and no oxazolones conversion compared to chlorides.
J. Coste et al.
Tetrahedron Letters, 32, 1967-1967 (1991)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 23955-5G-F | 04061833355145 |
