603130-12-7 Usage
Description
1,5-Anhydro-2,3,4-trideoxy-2-[[(1,1-dimethylethoxy)carbonyl]amino]-D-erythrohexitol is a complex organic compound with a unique molecular structure. It is characterized by the absence of hydroxyl groups at the 2nd, 3rd, and 4th carbon positions, and the presence of an amino group attached to a carbonyl group derived from 1,1-dimethylethoxy. 1,5-Anhydro-2,3,4-trideoxy-2-[[(1,1-diMethylethoxy)carbonyl]aMino]-D-erythrohexitol holds potential for various applications in different industries due to its specific chemical properties.
Uses
Used in Pharmaceutical Industry:
1,5-Anhydro-2,3,4-trideoxy-2-[[(1,1-dimethylethoxy)carbonyl]amino]-D-erythrohexitol is used as a reagent for the preparation of topoisomerase inhibitors. These inhibitors possess potent anti-gram-positive activity, making them valuable in the development of new antibiotics to combat gram-positive bacterial infections.
Used in Chemical Synthesis:
In the field of chemical synthesis, 1,5-Anhydro-2,3,4-trideoxy-2-[[(1,1-dimethylethoxy)carbonyl]amino]-D-erythrohexitol is utilized in the formation of dipeptide isoteres. These compounds are important intermediates in the synthesis of various biologically active peptides and may have potential applications in drug development and other related areas.
Check Digit Verification of cas no
The CAS Registry Mumber 603130-12-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,1,3 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 603130-12:
(8*6)+(7*0)+(6*3)+(5*1)+(4*3)+(3*0)+(2*1)+(1*2)=87
87 % 10 = 7
So 603130-12-7 is a valid CAS Registry Number.
603130-12-7Relevant articles and documents
3-AMINO-6-(1-AMINO-ETHYL)-TETRAHYDROPYRAN DERIVATIVES
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Page/Page column 38, (2009/01/24)
The invention relates to antibacterial compounds of formula I wherein R1 represents halogen or alkoxy; U and W each represent N, V represents CH and R2 represents H or F, or U and V each represent CH, W represents N and R2
Synthesis of novel tetrahydropyran-based dipeptide isosters by overman rearrangement of 2,3-didehydroglycosides
Kriek, Nicole M. A. J.,Van der Hout, Elise,Kelly, Paskal,Van Meijgaarden, Krista E.,Geluk, Annemieke,Ottenhoff, Tom H. M.,Van der Marel, Gijs A.,Overhand, Mark,Van Boom, Jacques H.,Valentijn, A. Rob P. M.,Overkleeft, Herman S.
, p. 2418 - 2427 (2007/10/03)
Differently functionalized tetrahydropyran-based dipeptide isosters have been efficiently synthesized from 3,4,6-tri-Oacetyl-D-glucal. Analogues of the hsp65 p2-13 epitope of Mycobacterium tuberculosis and Mycobacterium leprae were prepared by replacement of the Ala-Tyr or Glu-Glu moiety in the native dodecapeptide with the prepared dipeptide isosters. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
