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4921-08-8

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4921-08-8 Usage

Chemical group

Belongs to the phenothiazine group, which is commonly used as an antipsychotic medication.

Structural feature

Contains a trifluoromethyl group attached to the propanol.

Therapeutic effects

Known for its potential therapeutic effects in the treatment of mental disorders and schizophrenia.

Pharmacological properties

Has been studied for its ability to modulate the central nervous system and affect dopamine and serotonin receptors.

Research focus

Being researched for its potential use in treating other conditions such as anxiety, bipolar disorder, and depression.

Versatility

Shows promise as a versatile chemical compound with potential therapeutic applications in the field of psychopharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 4921-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4921-08:
(6*4)+(5*9)+(4*2)+(3*1)+(2*0)+(1*8)=88
88 % 10 = 8
So 4921-08-8 is a valid CAS Registry Number.

4921-08-8SDS

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 3-[2-(trifluoromethyl)phenothiazin-10-yl]propan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:4921-08-8 SDS

4921-08-8Downstream Products

4921-08-8Relevant articles and documents

Synthesis of deuterium-labeled fluphenazine

Shetty,Hawes,Midha

, p. 87 - 90 (2007/10/02)

The propylpiperazine side chain of fluphenazine has been labeled with two, four, and six deuterium atoms by lithium aluminum deuteride reduction of the appropriate ester or imide. The γ-carbon of the propyl group was labeled with two deuterium atoms by reduction of 10- (2-methoxycarbonylethyl)-2-trifluoromethyl-10H-phenothiazine, while four deuterium atoms were incorporated into the piperazine ring by reduction of 10-[3-(3,5-dioxo-1-piperazinyl)propyl]-2-trifluoro-methyl-10H-phenothiazin e. The latter reduction gave the d4-labeled N-deshydroxyethyl metabolite of fluphenazine.

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