All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C4H7NaO2S
Molecular Weight:
142.15
UNSPSC Code:
12352200
Recommended Products
form
powder or crystals
reaction suitability
reaction type: C-C Bond Formation
reaction type: C-H Activation
reagent type: catalyst
Application
The following Baran sulfinate is a part of a toolbox of diversification reagents, which are ideal for the late-stage functionalization of nitrogen-containing heterocycles. The regioselectivity can be effectively tuned by modification of the pH and solvent selection.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.
If you need assistance, please contact Customer Support.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Palladium-catalyzed coupling of vinyl tosylates with arylsulfinate salts.
Reeves D C, et al.
Tetrahedron Letters, 50(24), 2870-2873 (2009)
Pd (II)-Catalyzed Direct Sulfonylation of Unactivated C (sp3)?H Bonds with Sodium Sulfinates.
Rao W H, et al.
Organic Letters, 17(14), 3552-3555 (2015)
Copper-Catalyzed Aerobic Decarboxylative Sulfonylation of Cinnamic Acids with Sodium Sulfinates: Stereospecific Synthesis of (E)-Alkenyl Sulfones.
Jiang Q, et al.
The Journal of Organic Chemistry, 79(16), 7372-7379 (2014)
Cu-Catalyzed Deoxygenative C2-Sulfonylation Reaction of Quinoline N-Oxides with Sodium Sulfinate.
Du B, et al.
Organic Letters, 18(16), 4144-4147 (2016)
Active Filters
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
