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1027019-12-0

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1027019-12-0 Usage

Classification

Monoamine oxidase inhibitor (MAOI)

Medical Use

Treatment of depression and anxiety disorders

Mechanism of Action

Increases levels of serotonin and dopamine in the brain

Physical Form

White to off-white crystalline powder

Solubility

Soluble in water

Route of Administration

Orally in tablet form

Potential Drug Interactions

Can interact with certain foods, beverages, and other medications

Caution

Should only be used under the supervision of a healthcare professional

Check Digit Verification of cas no

The CAS Registry Mumber 1027019-12-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,0,1 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1027019-12:
(9*1)+(8*0)+(7*2)+(6*7)+(5*0)+(4*1)+(3*9)+(2*1)+(1*2)=100
100 % 10 = 0
So 1027019-12-0 is a valid CAS Registry Number.

1027019-12-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloro-2-ethyl-1,3-benzoxazole

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:1027019-12-0 SDS

1027019-12-0Downstream Products

1027019-12-0Relevant articles and documents

Organocatalytic syntheses of benzoxazoles and benzothiazoles using aryl iodide and oxone via C-H functionalization and C-O/S bond formation

Alla, Santhosh Kumar,Sadhu, Pradeep,Punniyamurthy, Tharmalingam

, p. 7502 - 7511 (2014/09/16)

An organocatalytic protocol for the syntheses of 2-substituted benzoxazoles and benzothiazoles is described from alkyl-/arylanilides and alkyl-/arylthioanilides using 1-iodo-4-nitrobenzene as catalyst and oxone as an inexpensive and environmentally safe terminal oxidant at room temperature in air via oxidative C-H functionalization and C-O/S bond formation. The procedure is simple and general and provides an effective route for the construction of functionalized 2-alkyl-/arylbenzoxazoles and 2-alkyl-/arylbenzothiazoles with moderate to high yields. The synthetic and mechanistic aspects have been described.

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