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1-(4-chlorobenzoyl)-N,5-dimethoxy-2-methyl-1H-indole-3-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127080-14-2

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127080-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127080-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,8 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127080-14:
(8*1)+(7*2)+(6*7)+(5*0)+(4*8)+(3*0)+(2*1)+(1*4)=102
102 % 10 = 2
So 127080-14-2 is a valid CAS Registry Number.

127080-14-2Downstream Products

127080-14-2Relevant academic research and scientific papers

N-Alkenylation of hydroxamic acid derivatives with ethynyl benziodoxolone to synthesizecis-enamides through vinyl benziodoxolones

Shimbo, Daisuke,Maruyama, Toshifumi,Tada, Norihiro,Itoh, Akichika

supporting information, p. 2442 - 2447 (2021/04/02)

The stereoselective synthesis ofcis-β-N-alkoxyamidevinyl benziodoxolones (cis-β-N-RO-amide-VBXs) fromO-alkyl hydroxamic acids in the presence of an ethynyl benziodoxolone-acetonitrile complex (EBX-MeCN) is reported herein. The reaction was performed under mild conditions including an aqueous solvent, a mild base, and room temperature. The reaction tolerated variousO-alkyl hydroxamic acids derived from carboxylic acids, such as amino acids, pharmaceuticals, and natural products. Vinyl dideuteratedcis-β-N-MeO-amide-VBXs were also synthesized using deuterium oxide as the deuterium source. Valine-derivedcis-β-N-MeO-amide-VBX was stereospecifically derivatized to hydroxamic acid-derivedcis-enamides without the loss of stereoselectivity or reduction in the deuterium/hydrogen ratio.

HYDROXAMATE DERIVATIVES OF SELECTED NONSTEROIDAL ANTIINFLAMMATORY ACYL RESIDUES AND THEIR USE FOR CYCLOOXYGENASE AND 5-LIPOXYGENASE INHIBITION

-

, (2008/06/13)

The present invention is novel selected hydroxamic acid derivatives of acyl residues of selected NSAIDS, i.e. having 5-lipoxygenase and cyclooxygenase inhibiting properties, pharmaceutical compositions for treating conditions advantageously affected by th

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