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19394-03-7

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19394-03-7 Usage

Chemical Class

Oxazolidine derivatives

Psychoactive Drug

Yes

Primary Use

Treatment of schizophrenia and other psychotic disorders

Mechanism of Action

Blocks dopamine receptors in the brain

Alleviates Symptoms

Hallucinations, delusions

Administration

Oral (tablets or liquid suspension)

Additional Uses

Treatment of acute mania, bipolar disorder, and adjunct treatment for depression

Combination Therapy

Can be used with other medications

Side Effects

Drowsiness, dizziness, extrapyramidal symptoms

Caution

Use with caution in patients with cardiovascular disease or abnormal heart rhythms.

Check Digit Verification of cas no

The CAS Registry Mumber 19394-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,9 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19394-03:
(7*1)+(6*9)+(5*3)+(4*9)+(3*4)+(2*0)+(1*3)=127
127 % 10 = 7
So 19394-03-7 is a valid CAS Registry Number.

19394-03-7SDS

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 2-(4-chlorophenyl)-3-ethyl-1,3-oxazolidine

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:19394-03-7 SDS

19394-03-7Relevant articles and documents

Thermal Rearrangement of some Oxazolidine N-Oxides. 2-Alkyl-6-aryl-3,4-dihydro-2H-1,5,2-dioxazines

Saba, Shahrokh,Domkowski, Patrick W.,Firooznia, Fariborz

, p. 921 - 923 (2007/10/02)

3-Alkyl-2-aryloxazolidines are oxidized with 3-chloroperoxybenzoic acid to produce the corresponding oxazolidine N-oxides.These N-oxides undergo thermal rearrangement to give 2-alkyl-6-aryl-3,4-dihydro-2H-1,5,2-dioxazines in 55-85 percent yield.

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