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5285-41-6

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5285-41-6 Usage

General Description

5,6-dichlorobenzoxazol-2(3H)-one is a chemical compound with the molecular formula C7H3Cl2NO2. It is a derivative of benzoxazolone, containing two chlorine atoms in the 5 and 6 positions of the benzene ring. 5,6-dichlorobenzoxazol-2(3H)-one is commonly used as a fluorescent tracer for the detection of oxidative stress in various biological samples. It can also be used as a chemical intermediate in the synthesis of other organic compounds. 5,6-dichlorobenzoxazol-2(3H)-one is typically handled and stored with care, as it is considered to be a hazardous substance with potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 5285-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,8 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5285-41:
(6*5)+(5*2)+(4*8)+(3*5)+(2*4)+(1*1)=96
96 % 10 = 6
So 5285-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl2NO2/c8-3-1-5-6(2-4(3)9)12-7(11)10-5/h1-2H,(H,10,11)

5285-41-6SDS

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 5,6-dichloro-3H-1,3-benzoxazol-2-one

1.2 Other means of identification

Product number -
Other names EINECS 226-121-0

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:5285-41-6 SDS

5285-41-6Relevant articles and documents

A method for synthesizing anti-mildew agent O

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Paragraph 0010; 0024; 0026; 0027, (2017/04/06)

The invention discloses a synthesis method of mildew preventive O. The synthesis method comprises the following steps: carrying out condensation reaction on 5-chloro-2-hydroxyaniline and urea under existence of hydrochloric acid to prepare 5-chlorobenzene oxazolone intermediate; carrying out substitution reaction on 5-chlorobenzene oxazolone, the hydrochloric acid and aqueous hydrogen peroxide solution under existence of polar solvent acetic acid, wherein the mass ratio of the 5-chlorobenzene oxazolone to the acetic acid to the hydrochloric acid to the aqueous hydrogen peroxide solution is 1 to 2.5 to 1.25 to 0.9; the reaction temperature is controlled at 50-75 DEG C; the reaction time is 3 hours; carrying out post-treatment such as cooling, washing and the like on the prepared product, so as to obtain a mildew preventive O crude product; recrystallizing by 95% of ethanol, so as to obtain a pure mildew preventive O product. The mildew preventive O is similar to white in appearance; the content is 96%; the melting point range is 185.0 DEG C to 187.0 DEG C; the product yield is over 80%.

BENZOXAZOLONE DERIVATIVES AS ACID CERAMIDASE INHIBITORS, AND THEIR USE AS MEDICAMENTS

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Page/Page column 40; 44, (2015/12/11)

The present invention relates to benzoxazolone derivatives as acid ceramidase inhibitors, pharmaceutical compositions containing these inhibitors and methods of inhibiting acid ceramidase for the treatment of disorders in which modulation of the levels of ceramide is clinically relevant. The invention also provides benzoxazolone derivatives for use as a medicament in the treatment of cancer, inflammation, pain, inflammatory pain or pulmonary diseases.

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