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1-Phenyl-4-(2-phenylhydrazono)pyrazolidine-3,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21272-26-4

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21272-26-4 Usage

Type of compound

Pyrazolone group of nonsteroidal anti-inflammatory drugs (NSAIDs)

Function

Inhibits the production of prostaglandins

Medical uses

Analgesic and antipyretic medication

Side effects

Potential to cause serious side effects such as agranulocytosis and aplastic anemia

Combination with other drugs

Often combined with paracetamol or codeine to enhance pain-relieving effects

Availability

No longer widely available in many countries due to potential side effects

Check Digit Verification of cas no

The CAS Registry Mumber 21272-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,7 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21272-26:
(7*2)+(6*1)+(5*2)+(4*7)+(3*2)+(2*2)+(1*6)=74
74 % 10 = 4
So 21272-26-4 is a valid CAS Registry Number.

21272-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl-pyrazolidinetrione 4-phenylhydrazone

1.2 Other means of identification

Product number -
Other names 1-Phenyl-3,4,5-trioxo-pyrazolidin-4-phenylhydrazon

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:21272-26-4 SDS

21272-26-4Downstream Products

21272-26-4Relevant academic research and scientific papers

Novel synthesis of highly functionalized pyrazolone systems via rearrangement of 5-phenyl-1-oxa-5,6-diazaspiro[2.4]heptane-4,7-diones

Metwally,Mohamed,Moustafa,El-Ossaily

experimental part, p. 1344 - 1353 (2011/10/17)

Epoxidation of 4-alkylidene(arylidene)-1-phenyl-3,5-pyrazolidinediones using alkaline hydrogen peroxide gave the corresponding 5-phenyl-1-oxa-5,6- diazaspiro[2.4]heptane-4,7-dione derivatives. Their reaction with nucleophilic reagents was investigated. The resulting products depend on the type of the diazaspiro compound and/or the nucleophile used.

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