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N-[[5-(2-fluorophenyl)-2,3-dihydro-1-methyl-1H-1,4-benzodiazepin-2-yl]methyl]thiophene-3-carboxamide is a complex chemical compound that belongs to the benzodiazepine class. It features a thiophene-3-carboxamide group and a 1-methyl-1H-1,4-benzodiazepin-2-yl group, which are connected by a methyl linker. N-[[5-(2-fluorophenyl)-2,3-dihydro-1-methyl-1H-1,4-benzodiazepin-2-yl]methyl]thiophene-3-carboxamide is characterized by its potential pharmacological properties, given the known sedative, hypnotic, anxiolytic, and muscle relaxant effects of benzodiazepines. The incorporation of a fluorophenyl group indicates a possible interaction with serotonin receptors, suggesting a broader spectrum of therapeutic applications.

83386-35-0

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83386-35-0 Usage

Uses

Used in Pharmaceutical Industry:
N-[[5-(2-fluorophenyl)-2,3-dihydro-1-methyl-1H-1,4-benzodiazepin-2-yl]methyl]thiophene-3-carboxamide is used as a potential candidate for the development of new drugs targeting the central nervous system. Its benzodiazepine nature suggests it may be effective for conditions requiring sedation, sleep induction, anxiety reduction, and muscle relaxation. The presence of the fluorophenyl group could enhance its activity at serotonin receptors, potentially broadening its therapeutic applications to include treatment of mood disorders and other conditions influenced by serotonin levels.
Used in Research and Development:
In the field of medicinal chemistry, N-[[5-(2-fluorophenyl)-2,3-dihydro-1-methyl-1H-1,4-benzodiazepin-2-yl]methyl]thiophene-3-carboxamide serves as a valuable compound for research into the structure-activity relationships of benzodiazepines and their derivatives. It can be used to explore the impact of specific structural modifications on the pharmacological profile of these compounds, potentially leading to the discovery of more effective and safer drugs.
Used in Drug Design and Optimization:
N-[[5-(2-fluorophenyl)-2,3-dihydro-1-methyl-1H-1,4-benzodiazepin-2-yl]methyl]thiophene-3-carboxamide is utilized in the process of drug design and optimization to create novel therapeutic agents with improved pharmacokinetic and pharmacodynamic properties. Its unique structure allows for the investigation of how different functional groups and molecular modifications can influence the compound's affinity, selectivity, and efficacy at specific biological targets, such as GABA receptors or serotonin receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 83386-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,8 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83386-35:
(7*8)+(6*3)+(5*3)+(4*8)+(3*6)+(2*3)+(1*5)=150
150 % 10 = 0
So 83386-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H20FN3OS/c1-26-16(13-25-22(27)15-10-11-28-14-15)12-24-21(17-6-2-4-8-19(17)23)18-7-3-5-9-20(18)26/h2-11,14,16H,12-13H2,1H3,(H,25,27)

83386-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Tifluadom

1.2 Other means of identification

Product number -
Other names 1-methyl-2-(3-thiophenecarbonyl)aminomethyl-5-(2'-fluorophenyl)-2,3-dihydro-1H-1,4-benzodiazepine

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:83386-35-0 SDS

83386-35-0Upstream product

83386-35-0Downstream Products

83386-35-0Relevant academic research and scientific papers

2-ACYLAMINOMETHYL-1,4-BENZODIAZEPINE DERIVATIVES AS CCK-ANTAGONISTS

-

, (2008/06/13)

A method of antagonizing the function of cholecystokinins in a disease state in mammals, especially in humans, which comprises administering a pharmaceutically-effective amount of certain 2-acylaminomethyl-1,4-benzodiazepine derivatives or their salts, alone or with a pharmaceutical carrier, with or without an adjuvant.

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