Ru(OAc)2[(R)-xylbinap] TCI R0170

Chemical Identity

CAS No.: 374067-50-2
PubChem: CID 164186537·SID 468592777
Formula: C56H54O4P2Ru
Molecular weight: 954.0 g/mol

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: bis(3,5-dimethylphenyl)-[1-[2-[(2,4-dimethylphenyl)-(3,5-dimethylphenyl)phosphanyl]naphthalen-1-yl]naphthalen-2-yl]phosphane;ruthenium(2+);diacetate
SMILES: CC1=CC(=C(C=C1)P(C2=C(C3=CC=CC=C3C=C2)C4=C(C=CC5=CC=CC=C54)P(C6=CC(=CC(=C6)C)C)C7=CC(=CC(=C7)C)C)C8=CC(=CC(=C8)C)C)C.CC(=O)[O-].CC(=O)[O-].[Ru+2]
InChIKey: LFKREVWNFUVXGI-UHFFFAOYSA-L

Rp 1.485.750,00

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Berat 200mg 1g

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Ru(OAc)2[(R)-xylbinap] is a chiral compound widely used in asymmetric synthesis as a catalyst or chiral reagent. It plays a crucial role in chemical reactions that require precise control over stereochemistry, particularly in the synthesis of compounds with specific structural configurations. This material is essential for producing molecules with defined stereochemical properties, which are vital in pharmaceutical and industrial applications. Its chiral nature allows for the selective formation of one enantiomer over another, enhancing reaction efficiency and reducing byproducts.

The compound’s chiral ligand, (R)-xylbinap, provides exceptional selectivity and reactivity in catalytic processes. Its complex structure, incorporating ruthenium metal and a chiral ligand, enables it to direct reactions with high stereoselectivity. This makes it a preferred choice for researchers aiming to achieve high yields and purity in asymmetric reactions. Additionally, its stability under certain conditions allows for repeated use in specific reactions, contributing to cost-effectiveness and sustainability in laboratory settings.

In Indonesian laboratories, Ru(OAc)2[(R)-xylbinap] is commonly used in organic chemistry research, especially in academic institutions focused on asymmetric synthesis. It supports the development of bioactive compounds, such as pharmaceuticals, by enabling precise control over molecular structure. Its application is particularly relevant in drug discovery and chemical synthesis, where stereochemistry plays a critical role in determining biological activity and efficacy.

Related TCI products

Asymmetric synthesis in pharmaceutical research for the production of chiral drugs with specific stereochemistry.
Organic chemistry experiments requiring precise control over reaction stereochemistry and enantiomeric purity.
Catalytic reactions in industrial chemical processes where selectivity and efficiency are critical factors.
Development of bioactive compounds, including pharmaceuticals and agrochemicals, through stereoselective pathways.
Research in green chemistry initiatives that aim to reduce waste and improve reaction efficiency using chiral catalysts.

Brand	TCI
CAS number	374067-50-2
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents
Pack sizes	50 g
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and light

Ru(OAc)2[(R)-xylbinap] should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air, which could affect its performance. Due to its chiral nature, it is important to handle the material with care to avoid contamination that might compromise its selectivity. In laboratory settings, it should be stored away from incompatible substances and in a well-ventilated area. Proper labeling and storage conditions ensure the material remains viable for multiple uses in research applications. Always follow standard safety protocols when handling chiral compounds to maintain a safe and efficient laboratory environment.

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