Skip to Content
Merck
All Photos(1)

Key Documents

51974

Sigma-Aldrich

Nonafluoro-1-butanesulfonyl chloride

≥98.0% ((GC))

Synonym(s):

Perfluoro-1-butanesulfonyl chloride

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4ClF9O2S
CAS Number:
Molecular Weight:
318.55
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98.0% ((GC))

SMILES string

FC(F)(F)C(F)(F)C(F)(F)C(F)(F)S(Cl)(=O)=O

InChI

1S/C4ClF9O2S/c5-17(15,16)4(13,14)2(8,9)1(6,7)3(10,11)12

InChI key

IRFCLLARAUQTNK-UHFFFAOYSA-N

Other Notes

Reagent for fluoro-tagging of nucleophiles

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

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

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.

Already Own This Product?

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

Visit the Document Library

C.W. Lindsley et al.
Tetrahedron Letters, 43, 4225-4225 (2002)
Moritz Baar et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(2), 526-530 (2014-11-22)
Heterogeneous catalysis for trifluoromethylations and perfluoroalkylations has been performed. Through the usage of cheap, metal-free and recyclable mesoporous graphitic carbon nitride (mpg-CN) it was possible to fluoroalkylate various arenes by the reductive activation of sulfonyl chlorides with visible light. Thus

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