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916257-05-1

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916257-05-1 Usage

Molecular Weight

267.32 g/mol

Structure

A pyrazole core with a carboxaldehyde group (-CHO) and a sulfonyl group (-SO2) attached to a 4-methylphenyl group.

Class

Pyrazole derivatives

Biological Activity

Potential applications in the development of new drugs and the study of molecular interactions and signaling pathways.

Use in Research

Commonly used in organic synthesis and pharmaceutical research.

Reactivity

Unique structure and reactivity make it a valuable building block for the synthesis of more complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 916257-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,2,5 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 916257-05:
(8*9)+(7*1)+(6*6)+(5*2)+(4*5)+(3*7)+(2*0)+(1*5)=171
171 % 10 = 1
So 916257-05-1 is a valid CAS Registry Number.

916257-05-1Downstream Products

916257-05-1Relevant articles and documents

An investigation into the role of 2,6-lutidine as an additive for the RuCl3-NaIO4 mediated oxidative cleavage of olefins to ketones

Watson, David W.,Gill, Matthew,Kemmitt, Paul,Lamont, Scott G.,Popescu, Mihai V.,Simpson, Iain

, p. 4479 - 4482 (2018)

2,6-Lutidine has been identified as a beneficial additive for the oxidative cleavage of olefins to ketones by NaIO4 in the presence of catalytic RuCl3, improving the yield and shortening the reaction times. In the absence of 2,6-lutidine reactions stalled at the diol intermediate with incomplete conversion to the desired ketones. The reaction protocol described herein also avoids the use of harmful solvents such as CCl4 and DCE and is tolerant of a range of functional groups.

AZAINDAZOLE COMPOUNDS AS CCR1 RECEPTOR ANTAGONISTS

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Page/Page column 217; 218, (2010/04/27)

Disclosed are compounds of the formula (I), useful for treating a variety of diseases and disorders that are mediated or sustained through the activity of CCR1 including autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis. Also disclosed are methods of making and methods of using same.

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