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2(3H)-Benzoxazolone, 5-chloro-6-(2-chlorobenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95637-40-4

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95637-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95637-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95637-40:
(7*9)+(6*5)+(5*6)+(4*3)+(3*7)+(2*4)+(1*0)=164
164 % 10 = 4
So 95637-40-4 is a valid CAS Registry Number.

95637-40-4SDS

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-chloro-6-(2-chlorobenzoyl)-3H-1,3-benzoxazol-2-one

1.2 Other means of identification

Product number -
Other names 2(3H)-Benzoxazolone,5-chloro-6-(2-chlorobenzoyl)

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:95637-40-4 SDS

95637-40-4Relevant academic research and scientific papers

3-Substituted piperazinomethyl benzoxazolinones. Analgesic and anti-inflammatory compounds inhibiting prostaglandin E2

Palaska,Unlu,Ozkanli,Pilli,Erdogan,Safak,Demirdamar,Gumusel,Duru

, p. 693 - 696 (2007/10/02)

Fourty-three new benzoxazolinone derivatives having a piperazinomethyl group at the third position of the ring were synthesized by using appropriate benzoxazolinones and 4-substituted piperazines via a Mannich reaction. The structures of the compounds were elucidated by spectral data and microanalyses. Analgesic activities were evaluated by a modified Koster test. All compounds, except 7, 14, 21, 32 and 41, showed analgesic activity higher than that of acetylsalicylic acid. The compounds were also screened for their anti-inflammatory activity using a carrageenan paw edema test, and those exhibiting high anti-inflammatory activity were investigated for their ability to inhibit prostaglandin E2 induced paw edema. The results of anti-inflammatory testing indicated that most of the compounds were more active than indomethacin. Ulcerogenic activities of the compounds were also studied and no gastrointestinal bleeding was observed at the 100 mg/kg dose level.

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