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(11bR,11′bR)-4,4′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis-dinaphtho[2,1-d:1′, 2′-f][1,3,2]dioxaphosphepin

CAS 349114-63-2C55H36O5P2Chemical Synthesis

(11bR,11′bR)-4,4′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis-dinaphtho[2,1-d:1′, 2′-f][1,3,2]dioxaphosphepin (CAS: 349114-63-2) is a chiral diphosphonite ligand with the molecular formula C55H36O5P2. This compound is primarily utilised as a specialised reagent in asymmetric synthesis, particularly for enantioselective hydrogenation reactions. Its unique structure facilitates high stereocontrol, making it valuable in producing chiral molecules for pharmaceutical and fine chemical industries.

IUPAC
R, R-Reetz X-Diphosphonite
Synonyms
9-Dimethyl-9H-xanthene-4,5-diyl)bis-dinaphtho[2,1-d:1′, 2′-f][1,3,2]dioxaphosphepin, 349114-63-2, C55H36O5P2, R, R-Reetz X-Diphosphonite
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(11bR,11′bR)-4,4′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis-dinaphtho[2,1-d:1′, 2′-f][1,3,2]dioxaphosphepin (C55H36O5P2) — chemical structure, CAS 349114-63-2; Chemistry, fine chemical supplied by Tech Serve Solutions
Asymmetric SynthesisChemical SynthesisChiral CatalystsLigandsand ReagentsHydrogenationReetz Ligands More...
01 /Applications

Asymmetric Transfer Hydrogenation

This diphosphonite ligand is effectively employed in Noyori-type asymmetric transfer hydrogenation of prochiral ketones. It enables the stereoselective reduction of carbonyl groups, yielding enantiomerically enriched alcohols.

Chiral Ligand in Catalysis

As a chiral catalyst ligand, it plays a crucial role in facilitating enantioselective transformations. Its application is key in the synthesis of chiral building blocks for complex organic molecules and pharmaceuticals.

Organic Synthesis Reagent

The compound serves as a vital reagent in advanced organic synthesis, particularly where precise control over stereochemistry is paramount. It contributes to the development of novel synthetic methodologies.

02 /Properties
Molecular weight838.82
Empirical formulaC55H36O5P2
Optical activity[α]22/D +270°, c = 1 in chloroform
ApplicationThis diphosphonite ligand has been successfully employed in Noyori-type asymmetric transfer hydrogenation of prochiral ketones.1
Melting point198-217 °C
03 /Identifiers & registry
CAS number
349114-63-2
04 /Quality & supply

Documentation

Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.

Supply & logistics

Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.

05 /Frequently asked questions

What is (11bR,11′bR)-4,4′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis-dinaphtho[2,1-d:1′, 2′-f][1,3,2]dioxaphosphepin used for?

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This compound is used as a chiral diphosphonite ligand in asymmetric synthesis, notably for Noyori-type asymmetric transfer hydrogenation of prochiral ketones.

What is the CAS number and formula for this chemical?

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The CAS number is 349114-63-2, and the empirical formula is C55H36O5P2.

What grade and purity does Tech Serve Solutions supply?

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Tech Serve Solutions supplies this compound as a research-grade chemical. We do not represent it as USP, BP, EP, or any other pharmacopoeia grade unless explicitly stated otherwise.

What are the safety and handling considerations for this product?

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This compound has a GHS classification indicating hazards. Refer to the Safety Data Sheet (SDS) for detailed information on handling, storage, and necessary personal protective equipment (PPE). Store in a cool, dry place.

How is this product packed, shipped, and exported?

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Tech Serve Solutions packs and ships this chemical in accordance with international regulations for hazardous materials. We are experienced global exporters of fine chemicals.

How can I request a sample or a quote?

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Please contact our sales team via the website or directly by email to request a sample or obtain a quotation for this product.

Need (11bR,11′bR)-4,4′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis-dinaphtho[2,1-d:1′, 2′-f][1,3,2]dioxaphosphepin in a specific grade or volume?