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(22E)-Stigmasta-5,22-dien-3β-ol trifluoroacetate is a chemical compound derived from stigmasterol, a naturally occurring plant sterol. It is characterized by the presence of a trifluoroacetic acid group attached to the 3β-hydroxyl group of the stigmasterol molecule. This modification enhances the solubility and stability of the compound, making it suitable for various applications in research and pharmaceuticals. The compound is known for its potential anti-inflammatory and immunosuppressive properties, which are being studied for their potential therapeutic benefits. Its chemical structure, with a double bond at the 22nd position and a trifluoroacetate group, distinguishes it from other stigmasterol derivatives and contributes to its unique properties and potential applications.

3870-50-6

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3870-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3870-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,7 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3870-50:
(6*3)+(5*8)+(4*7)+(3*0)+(2*5)+(1*0)=96
96 % 10 = 6
So 3870-50-6 is a valid CAS Registry Number.

3870-50-6Downstream Products

3870-50-6Relevant academic research and scientific papers

Photoredox-Catalyzed Defluorinative Functionalizations of Polyfluorinated Aliphatic Amides and Esters

Ye, Jian-Heng,Bellotti, Peter,Heusel, Corinna,Glorius, Frank

supporting information, (2022/01/20)

Selective C?F bond functionalization of perfluoalkyl units has huge potential towards accessing functionalized organofluorinated compounds, but remains challenging due to the high C?F bond strength and inherent selectivity challenges. We report a new catalytic approach to the selective functionalization of strong C?F bonds in polyfluorinated aliphatic esters and amides. This simple reaction proceeds in mild and operational fashion with divergent conversions, including hydrodefluorination, defluoroalkylation, and defluoroalkenylation, affording a diverse array of important partially fluorinated motifs. Straightforward downstream chemistry towards fluorinated alcohols, amines and drug derivatives highlights the potential of the protocol.

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