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Carbonic acid 4-((5R,5aR,8aS)-9-azido-6-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl)-2,6-dimethoxy-phenyl ester benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

197016-30-1

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197016-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197016-30-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,0,1 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 197016-30:
(8*1)+(7*9)+(6*7)+(5*0)+(4*1)+(3*6)+(2*3)+(1*0)=141
141 % 10 = 1
So 197016-30-1 is a valid CAS Registry Number.

197016-30-1Relevant academic research and scientific papers

HUMAN TOPOISOMERASE II-TARGETING ORGANOPLATINUM COMPOUNDS

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Paragraph 0117; 0119, (2020/03/15)

Some organoplatinum compounds have been synthesized. These organoplatinum compounds are designed to be human Topoisomerase II-targeting drugs.

ORGANOPLATINUM COMPOUNDS AND PHARMACEUTICAL COMPOSITION THEREOF AND METHOD OF PREPARING CRYSTAL OF hTop2

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Paragraph 0097; 0100, (2020/10/21)

Some organoplatinum compounds have been synthesized. These organoplatinum compounds are designed to be human Topoisomerase II-targeting drugs.

Stereo and chemoselective enzymatic reduction of azido functionality: Synthesis of 4-β-Aminopodophyllotoxin congeners by Baker's yeast

Kamal, Ahmed,Laxminarayana,Gayatri, N. Lakshmi

, p. 6871 - 6874 (2007/10/03)

4β-Aminopodophyllotoxin congeners have been synthesized by the stereoselective biocatalytic reduction of the 4-azidopodophyllotoxins employing baker's yeast in excellent yields under mild conditions.

Azepines by Photochemical Ring Enlargement of 9-Azidopodophyllotoxin- and 9-Azido-9'-demethylepipodophyllotoxin Derivatives

Laatsch, Hartmut,Ernst, Bernd Peter,Hoffmann, Dieter

, p. 1773 - 1778 (2007/10/03)

The azepines 5a-5c were obtained by photochemical nitrene rearrangement of the azides 1e/1f and 4b/4c in cyclohexene, but not in other solvents.They are ring expansion products of podophyllotoxin (1a) and resemble steganacin (9), but show only low biological activity.The triazenes 7a/8a and the aziridine 8b are also less active than 1a. - Keywords: Podophyllotoxin / Podophyllotoxin azides / Nitrene rearrangement

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