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1-(4-(AMinoMethyl)phenyl)-N,N-diMethylMethanaMine hydrochloride, commonly known as fluoxetine hydrochloride, is a medication that belongs to the selective serotonin reuptake inhibitors (SSRIs) class. It is used to treat various mental health conditions by increasing the levels of serotonin in the brain, which is believed to improve mood, appetite, and energy levels.

242452-35-3

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242452-35-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-(AMinoMethyl)phenyl)-N,N-diMethylMethanaMine hydrochloride is used as an antidepressant medication for treating mental health conditions such as depression, obsessive-compulsive disorder, and anxiety disorders. It helps restore the balance of serotonin in the brain, leading to an improvement in mood, appetite, and energy levels.
Used in Mental Health Treatment:
1-(4-(AMinoMethyl)phenyl)-N,N-diMethylMethanaMine hydrochloride is used as a therapeutic agent for managing the symptoms of mental health disorders. It is typically taken orally in the form of a tablet or liquid solution and should be used under the guidance of a healthcare professional to ensure proper dosage and monitoring of side effects, which may include nausea, headaches, and dizziness.

Check Digit Verification of cas no

The CAS Registry Mumber 242452-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,2,4,5 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 242452-35:
(8*2)+(7*4)+(6*2)+(5*4)+(4*5)+(3*2)+(2*3)+(1*5)=113
113 % 10 = 3
So 242452-35-3 is a valid CAS Registry Number.

242452-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-(aminomethyl)phenyl)-N,N-dimethylmethanamine hydrochloride

1.2 Other means of identification

Product number -
Other names 1-N,N-dimethylaminomethyl-4-aminomethylbenzene

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:242452-35-3 SDS

242452-35-3Relevant academic research and scientific papers

ALPHA 7 NICOTINIC ACETYLCHOLINE RECEPTOR ALLOSTERIC MODULATORS, THEIR DERIVATIVES AND USES THEREOF

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, (2016/09/26)

The present application is related to compounds represented by Formula I, which are novel positive allosteric modulators of α7 nAChRs. The application also discloses the treatment of disorders that are responsive to enhancement of acetylcholine action on α7 nAChRs in a mammal by administering an effective amount of a compound of Formula I.

NON-PEPTIDE GnRH AGENTS, METHODS AND INTERMEDIATES FOR THEIR PREPARATION

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Page/Page column 25, (2010/02/11)

Non-peptide GnRH agents capable of inhibiting the effect of gonadotropin-releasing hormone are described. Such compounds and their pharmaceutically acceptable salts, multimers, prodrugs, and active metabolites are suitable for treating mammalian reproductive disorders and steroid hormone-dependent tumors as well as for regulating fertility, where suppression of gonadotropin release is indicated. Methods for synthesizing the compounds and intermediates useful in their preparation are also described.

Non-peptide GnRH agents, methods and intermediates for their preparation

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Page/Page column 22-23, (2008/06/13)

Non-peptide GnRH agents capable of inhibiting the effect of gonadotropin-releasing hormone are described. Such compounds and their pharmaceutically acceptable salts, multimers, prodrugs, and active metabolites are suitable for treating mammalian reproductive disorders and steroid hormone-dependent tumors as well as for regulating fertility, where suppression of gonadotropin release is indicated. Methods for synthesizing the compounds and intermediates useful in their preparation are also described.

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