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1,4-Methanocyclopenta[c]pyrrole-1(2H)-carbonitrile,hexahydro-3a,6a-dimethyl-,(1R,3aS,4R,6aR)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

518314-75-5

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518314-75-5 Usage

Explanation

The compound consists of 8 carbon atoms, 13 hydrogen atoms, and 2 nitrogen atoms.

Explanation

The compound has a six-membered ring with a nitrogen atom and a carbonitrile functional group. It also contains two methyl groups (CH3) attached to the 3a and 6a positions of the ring.

Explanation

The stereochemistry of the compound is described by the (1R,3aS,4R,6aR) designation, which indicates the spatial arrangement of the atoms in the molecule.

Explanation

The compound contains a carbonitrile functional group (-CN) and two methyl groups (CH3) attached to the 3a and 6a positions of the ring.

Explanation

The compound has a six-membered ring structure, which is a common feature in many organic compounds.

Explanation

The compound is classified as a pyrrole derivative, which means it has an aromatic ring containing a nitrogen atom.

Explanation

The compound may have potential applications in various fields, such as medicinal chemistry, organic synthesis, or materials science. However, further research and analysis are needed to fully understand its properties and potential uses.

Explanation

The solubility of the compound in different solvents is not provided in the material, and it would require experimental data to determine.

Explanation

The stability of the compound under various conditions is not provided in the material, and it would require experimental data to determine.

Explanation

The reactivity of the compound with other chemicals or under different conditions is not provided in the material, and it would require experimental data to determine.

Molecular Structure

Hexahydro-3a,6a-dimethyl-1,4-methanocyclopenta[c]pyrrole-1(2H)-carbonitrile

Stereochemistry

(1R,3aS,4R,6aR)-(9CI)

Functional Groups

Carbonitrile, Methyl groups

Ring Size

Six-membered

Aromaticity

Pyrrole derivative

Potential Applications

Medicinal chemistry, organic synthesis, materials science

Solubility

Unknown

Stability

Unknown

Reactivity

Unknown

Check Digit Verification of cas no

The CAS Registry Mumber 518314-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,3,1 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 518314-75:
(8*5)+(7*1)+(6*8)+(5*3)+(4*1)+(3*4)+(2*7)+(1*5)=145
145 % 10 = 5
So 518314-75-5 is a valid CAS Registry Number.

518314-75-5Upstream product

518314-75-5Downstream Products

518314-75-5Relevant academic research and scientific papers

A chiral tricyclic proline analogue obtained from camphor

Gorichko, Marian V,Grygorenko, Oleksandr O,Komarov, Igor V

, p. 9411 - 9412 (2002)

Synthesis of 3a,6a-dimethylhexahydro-1,4-methanocyclopenta[c]pyrrole-1(2H)-carboxylic acid, a new chiral constrained proline analogue is reported. The synthesis was accomplished in five steps from 8-bromocamphor, easily available in both enantiomeric forms. A key step in the synthesis is an intramolecular 'domino'-type cyclisation, initiated by a nucleophile attack at an activated C=N bond.

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