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22494-47-9

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22494-47-9 Usage

General Description

Clobuzarit is a chemical compound that has been investigated for its potential use in the treatment of asthma. It is a leukotriene antagonist, which means it can block the action of certain compounds in the body that are involved in inflammatory and allergic reactions. By inhibiting the action of leukotrienes, clobuzarit may help to reduce inflammation in the airways and improve symptoms of asthma. However, further research is needed to determine the safety and effectiveness of clobuzarit for the treatment of asthma and other conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 22494-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,9 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22494-47:
(7*2)+(6*2)+(5*4)+(4*9)+(3*4)+(2*4)+(1*7)=109
109 % 10 = 9
So 22494-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H17ClO3/c1-17(2,16(19)20)21-11-12-3-5-13(6-4-12)14-7-9-15(18)10-8-14/h3-10H,11H2,1-2H3,(H,19,20)

22494-47-9SDS

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 2-[[4-(4-chlorophenyl)phenyl]methoxy]-2-methylpropanoic acid

1.2 Other means of identification

Product number -
Other names Clobuzaritum [INN-Latin]

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:22494-47-9 SDS

22494-47-9Downstream Products

22494-47-9Relevant articles and documents

Dioxolane derivatives

-

, (2008/06/13)

The invention is concerned with novel dioxolane derivatives of the formula: STR1 in which Ra is hydrogen or (1-4C)alkyl and Rb is (1-4C)alkyl or phenyl optionally bearing a halogeno substituent; their production; and their use for the manufacture of certain known anti-arthritic acids of the formula: STR2 and, in particular, those acids in which Ra =Rb =methyl or Ra =ethyl and Rb =phenyl, by a novel reduction process. The preferred reduction procedures involve the use of an alkali metal borohydride or cyanoborohydride in the presence of a noble metal catalyst, or the use of an α-branched alkyl or cycloalkyl Grignard agent. The use of the derivatives of formula I avoids the need for potentially toxic reagents and reactive intermediates in the previously known processes for the production of the acids of formula V.

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