38128-83-5 Usage
Description
(8Z,24E)-8-[(butoxyamino)methylidene]-5,6,17,19-tetrahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,9,11-trioxo-1,2,8,9-tetrahydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate is a complex organic compound that belongs to the class of naphthoquinones. It is a derivative of naphthoquinone and acetate, featuring multiple functional groups such as hydroxy, methoxy, epoxide, and acetate groups. The unique molecular structure and the presence of these functional groups suggest potential applications in various chemical and pharmaceutical fields.
Uses
Used in Pharmaceutical Industry:
(8Z,24E)-8-[(butoxyamino)methylidene]-5,6,17,19-tetrahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,9,11-trioxo-1,2,8,9-tetrahydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate is used as a potential pharmaceutical candidate for various applications due to its unique molecular structure and multiple functional groups.
Used in Chemical Industry:
In the chemical industry, (8Z,24E)-8-[(butoxyamino)methylidene]-5,6,17,19-tetrahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,9,11-trioxo-1,2,8,9-tetrahydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate may be utilized as a starting material or intermediate in the synthesis of other complex organic compounds, taking advantage of its diverse functional groups for further chemical reactions and modifications.
Check Digit Verification of cas no
The CAS Registry Mumber 38128-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,2 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38128-83:
(7*3)+(6*8)+(5*1)+(4*2)+(3*8)+(2*8)+(1*3)=125
125 % 10 = 5
So 38128-83-5 is a valid CAS Registry Number.
38128-83-5Relevant articles and documents
Oximes of 3 formylrifamycin SV. Synthesis, antibacterial activity, and other biological properties
Cricchio,Lancini,Tamborini,Sensi
, p. 396 - 403 (2007/10/06)
The synthesis of the oximes of 3 formylrifamycin SV and the preparation of some of the O substituted hydroxylamine intermediates are described. The chemical and physical characteristics, the antibacterial activity on wild type and rifampicin resistant strains, and other biological properties of the new derivatives are reported. Structure activity relationships show that increasing the lipophilicity of the oxime substituent decreases the antibacterial activity, both in vitro and in experimental infection, whereas inhibition of a rifampicin resistant strain of S. aureus and of several transcribing enzymes is increased.