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(αR,4S,9aβ)-Octahydro-6α-methyl-α-propyl-2H-quinolizine-4-ethanol benzoate is an alkaloid derived from the plant Poranthera corymbosa. It is typically isolated as a crystalline hydrobromide with a melting point of 251-252°C. The free base form of (αR,4S,9aβ)-Octahydro-6α-methyl-α-propyl-2H-quinolizine-4-ethanol benzoate is a colorless oil that exhibits levorotation with a specific rotation of [α]D -47° (CHCI3).

51105-10-3

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51105-10-3 Usage

Uses

Used in Pharmaceutical Industry:
(αR,4S,9aβ)-Octahydro-6α-methyl-α-propyl-2H-quinolizine-4-ethanol benzoate is used as a potential pharmaceutical compound for its various biological activities. (αR,4S,9aβ)-Octahydro-6α-methyl-α-propyl-2H-quinolizine-4-ethanol benzoate's unique structure and properties make it a candidate for further research and development in the field of drug discovery.
Used in Chemical Research:
(αR,4S,9aβ)-Octahydro-6α-methyl-α-propyl-2H-quinolizine-4-ethanol benzoate can also be utilized in chemical research as a starting material or a reference compound for the synthesis of other complex organic molecules. Its structural features may provide insights into the development of new chemical reactions or the study of reaction mechanisms.
Used in Analytical Chemistry:
(αR,4S,9aβ)-Octahydro-6α-methyl-α-propyl-2H-quinolizine-4-ethanol benzoate can be employed as a reference compound in analytical chemistry for the development and validation of analytical methods, such as high-performance liquid chromatography (HPLC) or gas chromatography (GC), for the separation and identification of similar alkaloids.
Used in Plant Biology and Ethnopharmacology:
(αR,4S,9aβ)-Octahydro-6α-methyl-α-propyl-2H-quinolizine-4-ethanol benzoate can be used in plant biology and ethnopharmacological studies to investigate the traditional uses of Poranthera corymbosa and other related plants. The study of its biological activities and potential therapeutic applications can contribute to the understanding of the plant's medicinal properties and the development of new treatments based on traditional knowledge.

References

Denne,!. Cryst. Mol. Struct., 3, 367 (1973) Johns et al., Austral. J. Chern., 27,2025 (1974)

Check Digit Verification of cas no

The CAS Registry Mumber 51105-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,0 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51105-10:
(7*5)+(6*1)+(5*1)+(4*0)+(3*5)+(2*1)+(1*0)=63
63 % 10 = 3
So 51105-10-3 is a valid CAS Registry Number.

51105-10-3Downstream Products

51105-10-3Relevant academic research and scientific papers

Stereoselective Synthesis of (+/-)-Porantheridine and (+/-)-Porantherilidine

Goessinger, Edda

, p. 783 - 788 (2007/10/02)

A variation of the recently described synthesis of porantherilidine leads to an intermediate, which can be converted to porantheridine as well as to porantherilidine. - Keywords: Natural products, total synthesis; (+/-)-Porantheridine, synthesis; (+/-)-Po

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