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(1R,5S)-8-Methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-ene is a complex azabicyclic compound with a unique molecular structure. It features a bicyclic ring system that incorporates a nitrogen atom, along with a methyl group at the 8th position, a phenyl group at the 3rd position, and a double bond at the 2nd position. (1R,5S)-8-Methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-ene holds potential for various applications in fields such as organic synthesis, pharmaceuticals, and as a component in more intricate molecular structures. Its distinct stereochemistry and structure may also render it a viable candidate for asymmetric synthesis and as a chiral ligand in catalytic reactions.

17814-96-9

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17814-96-9 Usage

Uses

Used in Organic Synthesis:
(1R,5S)-8-Methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-ene is utilized as a key intermediate in organic synthesis for the creation of more complex organic molecules. Its specific molecular architecture allows it to serve as a building block, facilitating the development of novel compounds with diverse applications.
Used in Pharmaceutical Industry:
Within the pharmaceutical sector, (1R,5S)-8-Methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-ene is employed as a potential active pharmaceutical ingredient. Its unique structure may contribute to the design of new drugs targeting specific biological pathways or receptors, offering therapeutic benefits in various medical conditions.
Used in Asymmetric Synthesis:
(1R,5S)-8-Methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-ene is used as a chiral building block in asymmetric synthesis. Its stereochemistry plays a crucial role in the production of enantiomerically pure compounds, which is essential in the development of drugs with fewer side effects and higher efficacy.
Used as a Chiral Ligand in Catalysis:
In the field of catalysis, (1R,5S)-8-Methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-ene is applied as a chiral ligand. Its presence can enhance the selectivity and efficiency of catalytic processes, leading to the production of desired enantiomers in an enantioselective manner, which is vital for the synthesis of high-quality pharmaceuticals and agrochemicals.
Further research and exploration into the properties and potential uses of (1R,5S)-8-Methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-ene may uncover additional applications, solidifying its role in the advancement of science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 17814-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,1 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17814-96:
(7*1)+(6*7)+(5*8)+(4*1)+(3*4)+(2*9)+(1*6)=129
129 % 10 = 9
So 17814-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H17N/c1-15-13-7-8-14(15)10-12(9-13)11-5-3-2-4-6-11/h2-6,9,13-14H,7-8,10H2,1H3

17814-96-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-methyl-3-phenyl-8-azabicyclo[3.2.1]oct-3-ene

1.2 Other means of identification

Product number -
Other names (1R,5S)-8-Methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-ene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17814-96-9 SDS

17814-96-9Relevant academic research and scientific papers

Substituted bridged phenyl piperidines: Orally active growth hormone secretagogues

Lu, Zhijian,Tata, James R.,Cheng, Kang,Wei, Liente,Chan, Wanda W.-S.,Butler, Bridget,Schleim, Klaus D.,Jacks, Thomas M.,Hickey, Gerard,Patchett, Arthur A.

, p. 1817 - 1820 (2007/10/03)

A new series of growth hormone secretagogues have been discovered. The best compound, 26j, shows excellent ability to release growth hormone both in vitro and in vivo. The synthesis and biological activity of these compounds are discussed.

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