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1H-1,4-Benzodiazepine, 2,3,4,5-tetrahydro-1-methyl- is a chemical compound belonging to the benzodiazepine class. It is characterized by a fused ring structure consisting of a diazepine ring (a seven-membered ring with two nitrogen atoms) and a benzene ring. The compound has a tetrahydro prefix, indicating that four hydrogen atoms have been added to the molecule, resulting in a saturated ring structure. The 1-methyl group is attached to the nitrogen atom at position 1, making it a substituted benzodiazepine. This class of compounds is known for its various biological activities, including sedative, hypnotic, and anxiolytic effects, and is widely used in the pharmaceutical industry for the development of drugs targeting the central nervous system.

4141-14-4

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4141-14-4 Usage

Chemical Class

Benzodiazepines

Explanation

1H-1,4-Benzodiazepine, 2,3,4,5-tetrahydro-1-methylbelongs to the class of benzodiazepines, which are a group of psychoactive drugs.

Explanation

1H-1,4-Benzodiazepine, 2,3,4,5-tetrahydro-1-methyl- has various psychoactive properties, including sedation, anxiety reduction, prevention of seizures, and muscle relaxation.

Explanation

The compound is structurally related to other benzodiazepines such as diazepam and alprazolam, which are also used for treating anxiety and other neurological disorders.

Explanation

Benzodiazepines, including 1H-1,4-Benzodiazepine, 2,3,4,5-tetrahydro-1-methyl-, act on the central nervous system by enhancing the activity of the neurotransmitter gamma-aminobutyric acid (GABA), which leads to a calming and relaxing effect on the body.

Explanation

The 2,3,4,5-tetrahydro-1-methyl-1H-1,4-benzodiazepine compound may be used in medical and scientific research to study its effects and potential applications.

Explanation

1H-1,4-Benzodiazepine, 2,3,4,5-tetrahydro-1-methyl- may be used in the development of pharmaceutical drugs for the treatment of various conditions, such as anxiety, insomnia, and other neurological disorders, due to its psychoactive properties and GABA-enhancing action.

Explanation

The compound is a tetrahydro derivative of 1-methyl-1H-benzodiazepine, which means it has four hydrogen atoms added to the benzene ring structure, making it more stable and potentially more effective.

Psychoactive Properties

Sedative, anxiolytic, anti-convulsant, and muscle relaxant

Structural Relation

Diazepam and Alprazolam

Central Nervous System Action

Enhancing GABA activity

Medical and Scientific Research

Potential use

Pharmaceutical Development

Treatment of anxiety, insomnia, and other neurological disorders

Tetrahydro Derivative

1-methyl-1H-benzodiazepine

Check Digit Verification of cas no

The CAS Registry Mumber 4141-14-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4141-14:
(6*4)+(5*1)+(4*4)+(3*1)+(2*1)+(1*4)=54
54 % 10 = 4
So 4141-14-4 is a valid CAS Registry Number.

4141-14-4Downstream Products

4141-14-4Relevant academic research and scientific papers

HISTONE ACETYLTRANSFERASE (HAT) INHIBITOR AND USE THEREOF

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Page/Page column 0043; 0046, (2021/02/25)

The present invention relates to a histone acetyltransferase (HAT) inhibitor. Provided are a compound represented by general formula I, a pharmaceutically acceptable salt, a stereoisomer, an enantiomer, a diastereomer, an atropisomer, a racemate, a polymorph, a solvate or an isotope-labeled compound (including deuterium substitution) thereof, a preparation method therefor, a pharmaceutical composition comprising the same, and use thereof in the treatment of various HAT-related diseases or conditions.

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