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Merck
CN

936111

SerrKap Palladacycle

greener alternative

≥95%, solid

别名:

[Pd(μ-AcO)(4-Cl-CˆN-SO3Na)]2

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关于此项目

经验公式(希尔记法):
C30H22Cl2N2Na2O10Pd2S2
化学文摘社编号:
分子量:
964.36
UNSPSC Code:
12352101
NACRES:
NA.21
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产品名称

SerrKap Palladacycle, ≥95%

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

assay

≥95%

form

solid

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

color

yellow

greener alternative category

storage temp.

−20°C

Quality Level

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

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.

hcodes

Hazard Classifications

Aquatic Chronic 4

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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

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