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474-48-6

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474-48-6 Usage

General Description

Reserpine N-oxide is a natural alkaloid and an active metabolite of reserpine, an indole alkaloid derived from the plant Rauwolfia serpentina. It is often used as a sedative and antipsychotic medication, primarily in the treatment of high blood pressure, anxiety, and mental disorders such as schizophrenia. Reserpine N-oxide works by acting on the central nervous system to decrease the levels of certain neurotransmitters, particularly dopamine and norepinephrine, which helps to regulate mood and behavior. The chemical structure of reserpine N-oxide consists of a tetracyclic alkaloid ring system with a series of functional groups that are responsible for its pharmacological effects. While it has demonstrated therapeutic potential, caution should be taken when using reserpine N-oxide due to its potential for side effects and interactions with other medications.

Check Digit Verification of cas no

The CAS Registry Mumber 474-48-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 474-48:
(5*4)+(4*7)+(3*4)+(2*4)+(1*8)=76
76 % 10 = 6
So 474-48-6 is a valid CAS Registry Number.

474-48-6SDS

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 11,17-dimethoxy-4-oxy-18-(3,4,5-trimethoxy-benzoyloxy)-yohimbane-16-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names ent-11,17β-dimethoxy-4-oxy-18α-(3,4,5-trimethoxy-benzoyloxy)-15β-yohimban-16α-carboxylic acid methyl ester

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:474-48-6 SDS

474-48-6Upstream product

474-48-6Downstream Products

474-48-6Relevant articles and documents

Indole cleavage with mebhydroline by sodium periodate. Part 1: Basic substituted indoles

Moehrle,Nestle,Westle

, p. 741 - 748 (2007/10/03)

The reaction behaviour of yohimbine (1), reserpine (5) and mebhydroline (7) as basic substituted indoles against periodate was examined. While 1 and 5 gave only the corresponding amine oxides 2 resp. 6 as definitive products, resulted from 7 beside the N-

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