(S)-N,N-Dimethyl-1-ferrocenylethylamine (L)-tartrate

98%

Reagent Code: #236303
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CAS Number 111614-65-4

science Other reagents with same CAS 111614-65-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 398.17 g/mol
Formula C₁₈H₂₅FeNO₆₁₀
badge Registry Numbers
MDL Number MFCD09953452
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its ferrocene backbone provides stability and stereochemical control, making it valuable in catalytic asymmetric reactions such as alkylations and aldol condensations. The tartrate salt form enhances solubility and crystallinity, facilitating purification and handling in synthetic routes. Commonly employed in organometallic chemistry and pharmaceutical research where precise stereochemistry is critical.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,640.00
inventory 25g
10-20 days ฿5,670.00
inventory 100g
10-20 days ฿18,810.00
(S)-N,N-Dimethyl-1-ferrocenylethylamine (L)-tartrate
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Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its ferrocene backbone provides stability and stereochemical control, making it valuable in catalytic asymmetric reactions such as alkylations and aldol condensations. The tartrate salt form enhances solubility and crystallinity, facilitating purification and handling in synthetic routes. Commonly employed in organometallic chemistry and pharmaceutical research where precise stereochemistr
Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its ferrocene backbone provides stability and stereochemical control, making it valuable in catalytic asymmetric reactions such as alkylations and aldol condensations. The tartrate salt form enhances solubility and crystallinity, facilitating purification and handling in synthetic routes. Commonly employed in organometallic chemistry and pharmaceutical research where precise stereochemistry is critical.
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