4840-12-4

Usage

Structure

Cyclopentene ring with an amine group and two methyl groups attached to the nitrogen atom.

Explanation

The compound has a five-membered carbon ring (cyclopentene) with a nitrogen atom bonded to one of the carbons. The nitrogen atom is also bonded to two methyl groups (CH3).

Explanation

The compound contains an amine group (-NH2), a cycloalkene ring (cyclic structure with alternating single and double bonds), and two alkyl groups (methyl groups, -CH3).

Explanation

Due to its unique structure, 1-Cyclopenten-1-amine, N,N-dimethylserves as a versatile building block for creating more complex organic molecules, particularly in the fields of pharmaceuticals and agrochemicals.

Explanation

The compound is known for its high reactivity, which makes it useful in various chemical reactions, especially in the formation of heterocyclic compounds.

Explanation

When handling 1-Cyclopenten-1-amine, N,N-dimethyl-, it is essential to take proper safety precautions to avoid skin and eye contact. Additionally, care should be taken to prevent ingestion or inhalation, as the compound may be harmful in these cases.

Explanation

The compound is also used as a reagent in various chemical reactions, further highlighting its versatility and importance in organic synthesis.

Functional Groups

Amine, Cycloalkene, and Alkyl groups.

Application

Building block in organic synthesis, used in pharmaceuticals and agrochemicals manufacturing.

Reactivity

Highly reactive.

Safety Precautions

Potential for skin and eye irritation, harmful if ingested or inhaled.

Usage

Reagent in chemical reactions.

InChI:InChI=1/C7H13N/c1-8(2)7-5-3-4-6-7/h5H,3-4,6H2,1-2H3

Upstream product

• 124-40-3 dimethyl amine 
• 120-92-3 cyclopentanone 
• 866-37-5 triethylgermyl dimethylamine 

Downstream Products

• 21695-39-6 1-phenyl-2-phenylimino-1,5,6,7-tetrahydro-2H-cyclopenta[d][1,3]thiazine-4-thione 
• 908095-51-2 2-<2'-(Benzenesulfonyl)-3'-oxobutyl>cyclopentanone 
• 1614-73-9 4-cycloheptene-1-carboxylic acid 
• 78089-76-6 trans-3,4-Dichloro-N-<<2-(dimethylamino)cyclopentyl>methyl>benzenamine 
• 78089-76-6 cis-3,4-Dichloro-N-<<2-(dimethylamino)cyclopentyl>methyl>benzenamine 
• 78089-80-2 trans-3',4'-Dichloro-2-(dimethylamino)cyclopentanecarboxanilide 
• 78089-78-8 cis-3',4'-Dichloro-N-<<2-(dimethylamino)cyclopentyl>methyl>propionanilide 
• 78089-82-4 trans-3',4'-Dichloro-N-<<2-(dimethylamino)cyclopentyl>methyl>propionanilide 
• 78089-81-3 (3,4-Dichloro-phenyl)-((1R,2S)-2-dimethylamino-cyclopentylmethyl)-amine; hydrochloride 
• 78089-77-7 (3,4-Dichloro-phenyl)-((1R,2R)-2-dimethylamino-cyclopentylmethyl)-amine; hydrochloride 
• 58712-11-1 methyl 3-(2-oxo-cyclopentyl)propanoate 
• 80419-42-7 2-(3-Methyl-benzthiazolin-2-yliden)cyclopentanon 
• 78089-79-9 cis-3',4'-Dichloro-2-(dimethylamino)cyclopentanecarboxanilide 
• 21695-38-5 1-phenyl-1,5,6,7-tetrahydro-cyclopenta[d][1,3]thiazine-2,4-dithione 

Relevant academic research and scientific papers

Diastereoselective Synthesis of Polycyclic Indolizines with 2-(2-Enynyl)pyridines and Enamines

A diastereoselective metal-catalyzed reaction of 2-(2-enynyl)pyridines and cyclic enamines is reported. The method provides access to a variety of substituted indolizine derivatives by variation of the enyne component and the reaction conditions. Performing the reaction using a preformed enamine led to the formation of polycyclic indolizines. With in situ generated enamines, ketone-containing indolizine derivatives were obtained. An asymmetric reaction of 2-(2-enynyl)pyridines and enamines generated from an aldehyde and a catalytic amount of amine is presented.

AN IMPROVED SYNTHESIS OF 4-CYCLOHEPTENE-1-CARBOXYLIC ACID

Modification of the method of Stork and Landesman (J.Am.Chem.Soc. 1956, 78, 5129) permitted the synthesis of the title acid (1) in 58 percent yield from a cylopentanone enamine.Acid 1 is a useful intermediate for the preparation of 4-substituted cycloheptenes in good yields.

Analgesic N-{2-[N'-(2-furylmethyl and 2-thienyl-methyl)-N'-alkylamino]cycloaliphatic}cyanobenzamides

Cis- and trans-N-(2-aminocycloaliphatic)benzamide compounds of the formula STR1 e.g., N-methyl-N-[2-(N-pyrrolidinyl)cyclohexyl]-3,4-dichlorobenzamide, and their pharmaceutically acceptable salts, have been found to have potent analgesic activity, and compositions containing these compounds useful in pharmaceutical dosage unit form for alleviating pain in warm blooded animals, as well as methods for alleviating pain in animals with these compositions. Processes for preparing the compounds are also disclosed.

Analgesic N-[2-(furyl-methylamino and 2-thienylmethylamino)cycloaliphatic]be

Cis - and trans-N-(2-aminocycycloaliphatic)benzamide compounds of the formula STR1 e.g., N-methyl-N-[2-[(2-furylmethyl)methylamino]-cyclohexyl]-3,4-dichlorobenzamide, and their pharmaceutically acceptable salts, have been found to have potent analgesic activity, and compositions containing these compounds useful in pharmaceutical dosage unit form for alleviating pain in warm-blooded animals, as well as methods for alleviating pain in animals with these compositions. Processes for preparing the compounds are also disclosed.

Analgesic N-(2-aminocycloaliphatic)benzamides

Cis- and trans-N-(2-aminocycloaliphatic)benzamide compounds of the formula STR1 E.G., N-methyl-N[2-(N-pyrrolidinyl)cyclohexyl[3,4-dichlorobenzamide, and their pharmaceutically acceptable salts, have been found to have potent analgesic activity, and compositions containing these compounds useful in pharmaceutical dosage unit form for alleviating pain in warm blooded animals, as well as methods for alleviating pain in animals with these compositions. Processes for preparing the compounds are also disclosed.