936111
SerrKap Palladacycle
≥95%
Synonym(s):
[Pd(μ-AcO)(4-Cl-CˆN-SO3Na)]2
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C30H22Cl2N2Na2O10Pd2S2
CAS Number:
Molecular Weight:
964.36
UNSPSC Code:
12352101
NACRES:
NA.21
Quality Level
Assay
≥95%
form
solid
color
yellow
storage temp.
−20°C
SMILES string
[H]C(C1=C([Pd]23oc(C)o[Pd]4(C5=C(C([H])=[N]4C6=CC=C(S(=O)(O[Na])=O)C=C6)C=CC(Cl)=C5)oc(C)o2)C=C(Cl)C=C1)=[N]3C7=CC=C(S(=O)(O[Na])=O)C=C7
Application
SerrKap Palladacycle is a phosphine-free, water soluble Pd dimer catalyst used extensively for low temperature modifications of nucleosides via Suzuki-Miyaura and Heck reactions. It is also compatible with flow reaction conditions and suitable for late-stage oligonucleotide and DNA modification.
related product
Product No.
Description
Pricing
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 4
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
新产品
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.
Santosh Kori et al.
Current protocols, 2(7), e502-e502 (2022-07-28)
Modification of nucleosides via cross-coupling processes has been carried out extensively on unprotected halonucleosides to produce functionalized nucleosides that are often developed for incorporation into oligonucleotides or used as fluorescent probes. This approach requires protection of the 5'-OH with the
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