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3-O-ethyloxazepam is a chemical compound belonging to the class of benzodiazepines, which are widely used as sedatives, hypnotics, and anticonvulsants. It is a derivative of oxazepam, with an ethyl group attached to the 3-hydroxyl position. This modification results in a more lipophilic compound, which may influence its pharmacokinetic properties, such as absorption, distribution, and elimination. 3-O-ethyloxazepam has been studied for its potential anxiolytic and muscle relaxant effects, although it is not as commonly prescribed as some other benzodiazepines due to its relatively weaker potency and shorter duration of action. Like other benzodiazepines, it works by enhancing the effect of the neurotransmitter gamma-aminobutyric acid (GABA) in the brain, leading to its calming and sedative effects. However, it also carries the risk of dependence and withdrawal symptoms, which has led to a more cautious approach to its clinical use.

4951-07-9

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4951-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4951-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,5 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4951-07:
(6*4)+(5*9)+(4*5)+(3*1)+(2*0)+(1*7)=99
99 % 10 = 9
So 4951-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H15ClN2O2/c1-2-22-17-16(21)19-14-9-8-12(18)10-13(14)15(20-17)11-6-4-3-5-7-11/h3-10,17H,2H2,1H3,(H,19,21)

4951-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-3-ethoxy-5-phenyl-1,3-dihydro-1,4-benzodiazepin-2-one

1.2 Other means of identification

Product number -
Other names 3-Etox

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:4951-07-9 SDS

4951-07-9Downstream Products

4951-07-9Relevant academic research and scientific papers

Acid-catalyzed ethanolysis of temazepam in anhydrous and aqueous ethanol solutions

Yang

, p. 898 - 902 (2007/10/02)

The benzodiazepines are a family of anxiolytic and hypnotic drugs. When taken concurrently with ethanol, a pharmacological interaction may occur, potentiating the central nervous system depression produced by either drug. In addition to this pharmacological interaction, this report describes a novel chemical reaction between temazepam (a 3-hydroxy-1,4-benzodiazepine) and ethanol under acidic conditions similar to those found in vivo, resulting in a 3-ethoxylated product. Optimal conditions, kinetics, equilibrium, and the mechanism of this acid-catalyzed ethanolysis are reported. The results raise the possibility that the ethanolysis reaction may occur in the stomach of people who consume alcohol and 3-hydroxy-1,4-benzodiazepine on a regular basis. The acid-catalyzed ethanol-drug reaction is a relatively unexplored area and may alter the pharmacological action of some drugs.

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