4075-49-4 Usage
Description
(24E)-5,6,9,17,19-pentahydroxy-8-[(2-hydroxyethyl)(methyl)amino]methyl-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate is a complex natural chemical compound that is a derivative of naphthoquinone. It features multiple hydroxy and methyl groups, an epoxide, and an acetate functional group within its long and intricate chemical structure. (24E)-5,6,9,17,19-pentahydroxy-8-[(2-hydroxyethyl)(methyl)amino]methyl-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate is likely to have significant pharmacological properties, making it a promising candidate for research and therapeutic applications.
Uses
Used in Pharmaceutical Research:
(24E)-5,6,9,17,19-pentahydroxy-8-[(2-hydroxyethyl)(methyl)amino]methyl-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate is used as a pharmaceutical research compound for its potential therapeutic applications. Its complex structure suggests that it may have unique properties that can be harnessed for the development of new drugs and treatments.
Used in Chemical Synthesis:
In the chemical industry, (24E)-5,6,9,17,19-pentahydroxy-8-[(2-hydroxyethyl)(methyl)amino]methyl-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate can be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique functional groups may enable the creation of novel molecules with specific applications in various fields.
Used in Material Science:
(24E)-5,6,9,17,19-pentahydroxy-8-[(2-hydroxyethyl)(methyl)amino]methyl-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate may also find applications in material science, where its unique structure could contribute to the development of new materials with specialized properties, such as improved stability, reactivity, or selectivity in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 4075-49-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4075-49:
(6*4)+(5*0)+(4*7)+(3*5)+(2*4)+(1*9)=84
84 % 10 = 4
So 4075-49-4 is a valid CAS Registry Number.
4075-49-4Relevant articles and documents
3-N-substituted aminomethyl derivatives of rifamycin SV. A convenient method of synthesis, cyclization of certain derivatives, and anticellular and antiviral activities of several derivatives
McCarthy,Moore,Wysong,Aldrich
, p. 1272 - 1276 (2007/10/21)
A new synthesis of Mannich bases of rifamycin SV using the Borch procedure with rifaldehyde is described. This new synthesis offers two advantages over the previously published method. It provides a route to monoalkyl-aminomethylrifamycins (1e-h) and to unsubstituted aminomethylrifamycins that were not accessible by the old procedure. The new method also offers a preparative route to Mannich bases 1a and 1b which were needed in multigram quantities for biological testing. In addition, the cyclization of certain of the monoalkylaminomethylrifamycins to the novel N,15 didehydro 15 deoxo 3,15 epi[methano(alkylimino)]rifamycin SV derivatives is described. The anticellular and antiviral effects of representatives of both series of compounds against cultured mouse cells and murine oncornavirus are discussed.
