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5-Chloro-3-ethylbenzoxazol-2(3H)-one is a chemical compound with the molecular formula C9H8ClNO2. It is a derivative of benzoxazol-2(3H)-one, featuring a chlorine atom at the 5th position and an ethyl group at the 3rd position. This heterocyclic compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound's properties, such as its solubility and stability, can be influenced by the presence of the chlorine and ethyl groups, making it a subject of interest in organic chemistry research and development.

5790-91-0

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5790-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5790-91-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,9 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5790-91:
(6*5)+(5*7)+(4*9)+(3*0)+(2*9)+(1*1)=120
120 % 10 = 0
So 5790-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H15FN2O3/c23-16-11-9-14(10-12-16)19-18(20(26)15-6-2-1-3-7-15)21(27)22(28)25(19)17-8-4-5-13-24-17/h1-13,19,26H/b20-18+

5790-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-3-ethyl-1,3-benzoxazol-2-one

1.2 Other means of identification

Product number -
Other names 2-BENZOXAZOLINONE,5-CHLORO-3-ETHYL

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:5790-91-0 SDS

5790-91-0Downstream Products

5790-91-0Relevant academic research and scientific papers

Electrogenerated N-heterocyclic carbenes: N-functionalization of benzoxazolones

Chiarotto,Feroci,Orsini,Sotgiu,Inesi

experimental part, p. 3704 - 3710 (2009/09/05)

A simple electrochemical procedure for the N-acylation and N-alkylation of benzoxazol-2(3H)-ones has been set up via electrolysis of an ionic liquid containing a benzoxazolone followed by addition of saturated or unsaturated anhydrides or alkyl halides. The electrochemically induced N-functionalization of benzoxazol-2(3H)-ones works very well in all tested ionic liquids, avoiding the use of volatile organic solvents. The N-acyl and N-alkyl derivatives of benzoxazol-2(3H)-ones were isolated in good to excellent yields; moreover, the ionic liquid has been reused fivefold maintaining the high yield of the products.

Benzimidazolone-, benzoxazolone-, or benzothiazolone derivatives as ion channel modulating agents

-

, (2008/06/13)

The present invention relates to ion channel modulating agents. More particularly, the present invention relates to a particular class of chemical compounds that has proven useful as modulators of SKCa, IKCa and BKCa channels. In further aspects, the present invention relates to the use of these SK/IK/BK channel modulating agents for the manufacture of medicaments, and pharmaceutical compositions comprising the SK/IK/BK channel modulating agents. The SK/IK/BK channel modulating agents of the invention are useful for the treatment or alleviation of diseases and conditions associated with the SK/IK/BK channels.

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