4840-12-4

Basic information

• Product Name: 1-Cyclopenten-1-amine,N,N-dimethyl-
• Synonyms: 1-Cyclopenten-1-amine,N,N-dimethyl-
• CAS NO: 4840-12-4
• Molecular Formula: C₇H₁₃N
• Molecular Weight: 0
• Mol File: 4840-12-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 154.8°Cat760mmHg
• Flash Point: 39.8°C
• Appearance: /
• Density: 0.88g/cm³
• Vapor Pressure: 3.12mmHg at 25°C
• Refractive Index: 1.486
• CAS DataBase Reference: 1-Cyclopenten-1-amine,N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Cyclopenten-1-amine,N,N-dimethyl-(4840-12-4)
• EPA Substance Registry System: 1-Cyclopenten-1-amine,N,N-dimethyl-(4840-12-4)

Safety Data

• Hazardous Substances Data: 4840-12-4(Hazardous Substances Data)

Usage

Structure

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

Explanation

Different sources of media describe the Explanation of 4840-12-4 differently. You can refer to the following data:
1. 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).
2. 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).
3. 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.
4. The compound is known for its high reactivity, which makes it useful in various chemical reactions, especially in the formation of heterocyclic compounds.
5. 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.
6. 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

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

Downstream Products

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

Relevant articles and documents

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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-(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.