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About This Item
Linear Formula:
FSO2C6H4COCl
CAS Number:
Molecular Weight:
222.62
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
206-949-9
MDL number:
Assay:
90%
grade
technical grade
Quality Level
assay
90%
reaction suitability
reaction type: click chemistry
bp
96-97 °C/0.7 mmHg (lit.)
mp
46-48 °C (lit.)
functional group
acyl chloride
SMILES string
FS(=O)(=O)c1ccc(cc1)C(Cl)=O
InChI
1S/C7H4ClFO3S/c8-7(10)5-1-3-6(4-2-5)13(9,11)12/h1-4H
InChI key
JMTAYFNTRRLWQG-UHFFFAOYSA-N
Application
4-(Fluorosulfonyl)benzoyl chloride was used as reagent in the synthesis of irreversible adenosine A1 antagonist 8-cyclopentyl-3-N-[3-((3-(4-fluorosulphonyl)benzoyl)-oxy)-propyl]-1-N-propyl-xanthine.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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J E van Muijlwijk-Koezen et al.
Bioorganic & medicinal chemistry letters, 11(6), 815-818 (2001-03-30)
A new preparative synthetic route for the irreversible adenosine A1 antagonist 8-cyclopentyl-3-N-[3-((3-(4-fluorosulphonyl)benzoyl)-oxy)-propyl]-1-N-propyl-xanthine (FSCPX, 1) is described. The availability of ample amounts of the irreversible antagonist FSCPX allowed us to use FSCPX as a research tool for adenosine A1 receptors in
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 136387-1G | 04061826197837 |

