Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

136387

Sigma-Aldrich

4-(Fluorosulfonyl)benzoyl chloride

technical grade, 90%

Synonym(s):

p-(Fluorosulfonyl)benzoyl chloride

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
FSO2C6H4COCl
CAS Number:
402-55-1
Molecular Weight:
222.62
EC Number:
206-949-9
MDL number:
MFCD00007419
UNSPSC Code:
12352100
PubChem Substance ID:
24848279
NACRES:
NA.22

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

Signal Word

Danger

Hazard Statements

H302,H314,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCN4914
MKBZ8238V
07721BG
06023LV

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Benzoyl chloride ReagentPlus®, ≥99%

Sigma-Aldrich

B12695

Benzoyl chloride

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service