Skip to Content
Merck
All Photos(1)

Documents

562610

Sigma-Aldrich

Nonafluorobutanesulfonic anhydride

97%

Synonym(s):

Nonafluorobutanesulfonic acid anhydride, Perfluorobutanesulfonic anhydride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CF3(CF2)3SO2)2O
CAS Number:
Molecular Weight:
582.18
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.3210 (lit.)

bp

84 °C (lit.)

density

1.898 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI

1S/C8F18O5S2/c9-1(10,5(17,18)19)3(13,14)7(23,24)32(27,28)31-33(29,30)8(25,26)4(15,16)2(11,12)6(20,21)22

InChI key

QKIHLPFZYGFMDK-UHFFFAOYSA-N

General description

Nonafluorobutanesulfonic anhydride can be synthesized by using potassium nonafluorobutane-sulfonate as the starting material.

Application

Nonafluorobutanesulfonic anhydride can play the role of an activating agent in the synthesis of 4-bromothieno[2,3-b]pyridine via reaction with tetra-n-butylammonium bromide in dichloromethane.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Skin Corr. 1B

Supplementary Hazards

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

"Towards highly activating leaving groups: studies on the preparation of some halogenated alkyl sulfonates"
Netscher T and Bohrer P
Molecules (Basel), 7(8), 601-661 (2002)
"Synthesis of 4-Arylthieno [2, 3-b] pyridines and 4-Aminothieno [2, 3-b] pyridines via a Regioselective Bromination of Thieno [2, 3-b] pyridine"
Lucas CCM, et al.
The Journal of Organic Chemistry, 80(24), 12594-12598 (2015)

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