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dibenzyl [4,17-dimethyl-3,6,10,13,16,19,23,26-octaoxo-11,24-di(propan-2-yl)-9,22-dioxa-28,29-dithia-2,5,12,15,18,25-hexaazabicyclo[12.12.4]triacontane-7,20-diyl]biscarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63520-00-3

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63520-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63520-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,2 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63520-00:
(7*6)+(6*3)+(5*5)+(4*2)+(3*0)+(2*0)+(1*0)=93
93 % 10 = 3
So 63520-00-3 is a valid CAS Registry Number.

63520-00-3Relevant academic research and scientific papers

Solution-phase synthesis of nucleobase-substituted analogues of triostin A

Lorenz, Katrin B.,Diederichsen, Ulf

, p. 3917 - 3927 (2007/10/03)

A synthesis of novel analogues of triostin A presenting two identical or different nucleobases instead of the original quinoxaline substituents has been developed. The DNA bisintercalator triostin A (1) with its rigid backbone provides an optimal scaffold

Synthesis and biological activity of new quinoxaline antibiotics of echinomycin analogues

Kim, Yun Bong,Kim, Yong Hae,Park, Ju Youn,Kim, Soo Kie

, p. 541 - 544 (2007/10/03)

Novel quinoxaline antibiotics having the methylenedithioether bridge as an analogue of echinomycin have been synthesized by insertion of methylene moiety between -S-S- bond. The compound 1a shows remarkable cytotoxicities against human tumor various cell

SYNTHESIS OF DES-N-TETRAMETHYLTRIOSTIN A FROM C-TERMINAL Z-D-SERINE TETRA- AND OCTADEPSIPEPTIDE INTERMEDIATES

Dhaon, Madhup K.,Gardner, Joseph H.,Olsen, Richard K.

, p. 57 - 62 (2007/10/02)

Des-N-tetramethyltriostin A (1), a known DNA-intercalation agent, has been synthesized from tetra- and octapeptide intermediates that have Z-D-serine at the C-terminal position.The procedure thus allows the fragment coupling and cyclization reactions lead

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