Bis(dibenzylideneacetone)palladium(0) TCI B1374

Chemical Identity

CAS No.: 32005-36-0
PubChem: CID 44630136·SID 87564299
Formula: C34H28O2Pd
Molecular weight: 575.0 g/mol

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (1Z,4E)-1,5-diphenylpenta-1,4-dien-3-one;(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one;palladium
SMILES: C1=CC=C(C=C1)/C=C/C(=O)/C=C/C2=CC=CC=C2.C1=CC=C(C=C1)/C=C/C(=O)/C=C\C2=CC=CC=C2.[Pd]
InChIKey: UKSZBOKPHAQOMP-HIBFLRMTSA-N

Rp 2.384.550,00

~~Rp 1.683.150,00~~ Rp 2.384.550,00

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Bis(dibenzylideneacetone)palladium(0) is an organopalladium compound widely used in catalytic chemical reactions, particularly in C-H activation processes. This material plays a crucial role in laboratory settings by acting as an efficient catalyst for various reactions, including coupling and cross-coupling reactions. Its ability to facilitate complex chemical transformations makes it an essential component in modern synthetic chemistry. The compound is especially valuable for its stability and reactivity, allowing it to be used in a wide range of experimental conditions. Its versatility and effectiveness have made it a go-to choice for researchers working with metal-based catalysts.

The compound’s high reactivity and stability under controlled conditions make it a preferred choice for laboratory applications. It exhibits excellent compatibility with a variety of organic substrates, enabling efficient and selective chemical transformations. Its structural complexity allows for strong interactions with target molecules, enhancing reaction efficiency. Additionally, its chemical stability during storage and use ensures minimal degradation, making it reliable for long-term research applications. These properties contribute to its popularity in both organic and inorganic chemical studies.

In Indonesian laboratories, Bis(dibenzylideneacetone)palladium(0) is commonly used in organic chemistry research. It is particularly favored for its role in catalytic reactions that require high selectivity and efficiency. Its application in reactions such as Suzuki-Miyaura and Heck has made it a staple in chemical synthesis processes. Researchers in Indonesia rely on this compound for its consistent performance and reliability in various experimental setups.

TCI brochures (PDF)

Thianthrenium Salt Useful for Electrophilic Vinylation 2023-09-29 · p. 1
Trifluoroborate Salts for Direct Introduction of Hydroxymethyl Group and Aminomethyl Group 2026-01-05 · p. 1
Palladium Catalysts for Cross-Coupling Reaction 2025-05-01 · p. 1
C-H Bond Activation Reaction 2025-06-20 · p. 4
Transition Metal Catalysts 2026-04-10 · p. 13
Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 23

Related TCI products

C-H Activation Reactions: This compound is ideal for C-H activation due to its ability to efficiently activate carbon-hydrogen bonds, making it suitable for complex organic transformations.
Cross-Coupling Reactions: Its high reactivity allows it to facilitate cross-coupling reactions, which are essential in the synthesis of diverse organic compounds.
Organic Synthesis: It is widely used in organic synthesis for its catalytic efficiency and compatibility with a range of substrates, enabling the production of various chemical compounds.
Metal-Based Catalysis: Its role as a metal-based catalyst makes it suitable for reactions requiring precise control over reaction pathways and selectivity.
Research and Development: It is a key component in R&D settings where efficient and selective catalytic reactions are required for new compound development.

From the TCI brochure

Palladium catalyst (cat.) in Suzuki-Miyaura type cross-coupling scheme with E1521

Brand	TCI
CAS number	32005-36-0
Molecular formula	—
Purity	—
Category	Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis]
Pack sizes	Available in various pack sizes as per supplier specifications
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and light

This compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and exposure to air. Due to its reactivity, it should be handled with care, and appropriate personal protective equipment should be worn when working with it. The compound is not flammable but should be stored away from incompatible materials. Regular inspection of storage conditions ensures its continued effectiveness in laboratory applications. Proper storage and handling practices are essential to maintain its catalytic properties and ensure safe usage in research settings.

References cited in the TCI brochure

Norio Murai. Palladium-Catalyzed Direct Hydroxymethylation of Aryl Halides and Triflates with Potassium Acetoxymethyltrifluoroborate Organic Letters, 2012. doi:10.1021/ol300149b