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2234-09-5

10-methyl-10H-phenothiazine 5-oxide, also known as methaqualone, is a chemical compound with the molecular formula C16H13N2S. It is a sedative-hypnotic drug that was once widely used as a treatment for insomnia and anxiety. However, due to its high potential for abuse and addiction, as well as severe side effects such as hallucinations and organ damage, methaqualone has been banned in many countries, including the United States. The compound is characterized by its phenothiazine structure, with a methyl group at the 10th position and an oxide group at the 5th position, which contributes to its pharmacological properties. Despite its historical use, methaqualone is now considered a dangerous substance and is not recommended for medical use.

2234-09-5

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2234-09-5 Usage

Physical Properties

Blue color

Uses

Dye for textiles, biological stain for microscopic examination of cells

Medicinal Uses

Treatment for malaria, methemoglobinemia, and urinary tract infections

Mechanism of Action

Enters cells and binds to structures such as DNA, affecting cell function

Potential Uses

Treatment of neurological conditions such as Alzheimer's disease and Parkinson's disease.

Check Digit Verification of cas no

The CAS Registry Mumber 2234-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,3 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2234-09:
(6*2)+(5*2)+(4*3)+(3*4)+(2*0)+(1*9)=55
55 % 10 = 5
So 2234-09-5 is a valid CAS Registry Number.

2234-09-5SDS

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 10-Methylphenothiazine 5-oxide

1.2 Other means of identification

Product number -
Other names thionyl amide

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:2234-09-5 SDS

2234-09-5Relevant articles and documents

Electron Transfer to Excited Doublet States. Photoirradiation of 10-Methylphenothiazine Cation Radical Perchlorate in Solutions of Phenylacetylene and p-Tolylacetylene in Acetonitrile

Shine, Henry J.,Zhao, Da-Chuan

, p. 4086 - 4089 (2007/10/02)

10-Methylphenothiazine cation radical perchlorate (MP.+ClO4-) underwent slow reaction with p-tolylacetylene (PTA) and phenylacetylene (PA) in solution in acetonitrile in the dark.Perchlorate salts (3a and 3b) assumed to be bis-adducts of MP.+ClO4- to the alkyne were formed.In contrast, irradiation of such solutions with visible light (λ > 400 nm) caused oxidation of the alkyne. 2-Methyl-3,6-di-p-tolylpyridine (1a) and 1,4-di-p-tolyl-5,6-dioxa-1,3-cyclohexadiene (2a) were formed from PTA, whereas 2-methyl-3,6-diphenylpyridine (1b) and 1-phenylnaphthalene (4b) were formed from PA.Irradiation of a solution of MP.+ClO4- and 1-pentyne gave only a trace of 2-methyl-3,6-dibutylpyridine (1c).

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