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3,4-dihydro-1-[(4-methoxyphenyl)methyl]-1H-1,4-Benzodiazepine-2,5-dione, commonly known as flurazepam, is a benzodiazepine medication primarily used for the treatment of insomnia. It functions by enhancing the effects of the neurotransmitter gamma-aminobutyric acid (GABA) in the brain, which helps to reduce the overactivity of certain brain cells and induce a calming effect. As a long-acting benzodiazepine, flurazepam has a relatively long half-life, allowing it to remain in the body for an extended period. Due to its potential for abuse and addiction, as well as its sedative effects, it is typically prescribed for short-term use and should be used with caution, particularly in individuals with a history of substance abuse or when used in conjunction with other central nervous system depressants.

169504-53-4

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169504-53-4 Usage

Uses

Used in Pharmaceutical Industry:
3,4-dihydro-1-[(4-methoxyphenyl)methyl]-1H-1,4-Benzodiazepine-2,5-dione is used as a medication for the treatment of insomnia due to its ability to enhance the effects of GABA, leading to a calming effect and promoting sleep.
Used in Sleep Aid Applications:
Flurazepam is used as a sleep aid for individuals suffering from insomnia, helping to reduce the overactivity of certain brain cells and induce a calming effect that facilitates sleep.
Used in Short-term Treatment:
Due to its potential for abuse and addiction, as well as its sedative effects, 3,4-dihydro-1-[(4-methoxyphenyl)methyl]-1H-1,4-Benzodiazepine-2,5-dione is used for short-term treatment of insomnia, ensuring that patients receive the necessary relief without the risk of long-term dependency.
Used with Caution in Substance Abuse History:
Flurazepam is used with caution in individuals with a history of substance abuse, as its potential for abuse and addiction may pose a risk to these patients. Careful monitoring and dosage adjustments may be necessary to ensure safe and effective treatment.
Used in Combination with Other CNS Depressants:
When used in conjunction with other central nervous system depressants, 3,4-dihydro-1-[(4-methoxyphenyl)methyl]-1H-1,4-Benzodiazepine-2,5-dione requires careful consideration and monitoring, as the combined sedative effects may increase the risk of adverse reactions or complications.

Check Digit Verification of cas no

The CAS Registry Mumber 169504-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,5,0 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 169504-53:
(8*1)+(7*6)+(6*9)+(5*5)+(4*0)+(3*4)+(2*5)+(1*3)=154
154 % 10 = 4
So 169504-53-4 is a valid CAS Registry Number.

169504-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-methoxyphenyl)methyl]-3,4-dihydro-1,4-benzodiazepine-2,5-dione

1.2 Other means of identification

Product number -
Other names 1-(4-Methoxybenzyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

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:169504-53-4 SDS

169504-53-4Downstream Products

169504-53-4Relevant academic research and scientific papers

BENZODIAZEPINE COMPOUNDS USEFUL FOR THE TREATMENT OF HEPATITIS C

-

, (2011/12/14)

The invention concerns benzodiazepine derivatives of Formula (I) wherein A, X, L1, L2, R1, R2, R3, R4, R5, R6 and R7 are as defined in the description. The present invention also relates to processes for the preparation of such compounds, pharmaceutical compositions containing them and their use in the treatment or prophylaxis of hepatitis C virus infection.

New synthesis of 1,3-dihydro-1,4-benzodiazepin-2(2H)-ones and 3-amino-1,3-dihydro-1,4-benzodiazepin-2(2H)-ones: Pd-catalyzed cross-coupling of imidoyl chlorides with organoboronic acids

Nadin, Alan,Sanchez Lopez, Jose M.,Owens, Andrew P.,Howells, Dean M.,Talbot, Adam C.,Harrison, Timothy

, p. 2844 - 2852 (2007/10/03)

A new approach to the synthesis of 1,4-benzodiazepines and 3-amino-1,4-benzodiazepines, which employs the Pd-catalyzed cross-coupling reaction of an imidoyl chloride with an organometallic reagent as the key step, is described. A five-step synthesis of a

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