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136387

4-(氟磺酰)苯酰氯

technical grade, 90%

别名:

p-(Fluorosulfonyl)benzoyl chloride

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关于此项目

线性分子式:
FSO2C6H4COCl
化学文摘社编号:
402-55-1
分子量:
222.62
NACRES:
NA.22
PubChem Substance ID:
24848279
UNSPSC Code:
12352100
EC Number:
206-949-9
MDL number:
MFCD00007419
Assay:
90%
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grade

technical grade

Quality Level

100

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.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

存储类别

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCN4914
MKBZ8238V
07721BG
06023LV

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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

全球贸易项目编号

货号GTIN
136387-1G04061826197837