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729-89-5

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729-89-5 Usage

General Description

Medifoxamine acid metabolite is a chemical compound that is produced in the body as a metabolite of the drug medifoxamine. Medifoxamine is a psychoactive drug that is used as an antidepressant and anxiolytic medication. The acid metabolite of medifoxamine is generated through metabolic processes in the body and is responsible for the therapeutic effects of the drug. It is thought to act by modulating the levels of serotonin and other neurotransmitters in the brain, leading to improvements in mood and reduction in anxiety symptoms. Overall, the medifoxamine acid metabolite plays a crucial role in the pharmacological actions of the drug medifoxamine and its effectiveness in treating depression and anxiety disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 729-89-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 729-89:
(5*7)+(4*2)+(3*9)+(2*8)+(1*9)=95
95 % 10 = 5
So 729-89-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O4/c15-13(16)14(17-11-7-3-1-4-8-11)18-12-9-5-2-6-10-12/h1-10,14H,(H,15,16)

729-89-5SDS

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 2,2-diphenoxyacetic acid

1.2 Other means of identification

Product number -
Other names EINECS 211-981-1

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:729-89-5 SDS

729-89-5Relevant articles and documents

Synthesis of New Aryloxyacetic Acid Derivatives

Colin, J.L.,Loubinoux, B.

, p. 568 - 571 (2007/10/02)

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