(S)-4-tert-Butyl-2-[(SP)-2-(diphenylphosphino)ferrocenyl]-2-oxazoline
(S)-4-tert-Butyl-2-[(SP)-2-(diphenylphosphino)ferrocenyl]-2-oxazoline (CAS 163169-15-1) is a sophisticated organometallic compound featuring a ferrocene backbone with a chiral oxazoline ligand. With a molecular weight of 495.37 g/mol and empirical formula C29H30FeNOP, it is primarily employed as a highly effective chiral ligand in asymmetric synthesis. Its unique structure facilitates enantioselective catalysis, making it invaluable for producing chiral molecules with high optical purity.
- IUPAC
- (2R)-1-[(4S)-4-(1,1-Dimethylethyl)-4,5-dihydro-2-oxazolyl]-2-(diphenylphosphino)ferrocene (acc to CAS),Naud ligand SL-N004-2
![(S)-4-tert-Butyl-2-[(SP)-2-(diphenylphosphino)ferrocenyl]-2-oxazoline (C29H30FeNOP) — chemical structure, CAS 163169-15-1; Chemistry, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F163169-15-1.png&w=3840&q=75)
Asymmetric Catalysis
This ferrocene-oxazoline ligand is a key component in transition metal-catalyzed asymmetric reactions. It enables the selective formation of one enantiomer over the other, crucial for pharmaceutical synthesis.
Chiral Ligand Design
Its well-defined stereochemistry and phosphine donor atom make it an excellent building block for designing custom chiral catalysts for specific synthetic challenges.
Organic Synthesis
Used to promote enantioselective transformations, such as additions, cyclisations, and reductions, leading to the creation of complex chiral organic molecules.
| Molecular weight | 495.37 |
|---|---|
| Empirical formula | C29H30FeNOP |
| Assay | ≥97% |
| Optical purity | ee: ≥99% |
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.
What is (S)-4-tert-Butyl-2-[(SP)-2-(diphenylphosphino)ferrocenyl]-2-oxazoline used for?
+
It is primarily used as a chiral ligand in asymmetric synthesis and catalysis to promote enantioselective reactions.
What is the CAS number and formula for this compound?
+
The CAS number is 163169-15-1 and the empirical formula is C29H30FeNOP.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies this product with an assay of ≥97% and optical purity (ee) of ≥99%. It is supplied as a research grade chemical and is not represented as USP, BP, EP, or other pharmacopoeia grades.
How should this chemical be handled safely?
+
This compound is classified under WGK Germany 3. Handle with appropriate personal protective equipment in a well-ventilated area. Avoid contact with skin, eyes, and clothing, and do not ingest or inhale.
How is this product packed and shipped?
+
Products are carefully packed according to international regulations for hazardous materials. We export globally, ensuring compliance with all relevant shipping requirements.
How can I request a sample or a quote?
+
Please contact our sales team via the website or email to request a sample or obtain a quotation for this product.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis