38129-09-8 Usage
Uses
Used in Pharmaceutical Industry:
(14E,24E)-8-[(ethylamino)methyl]-5,6,9,17,19-pentahydroxy-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 potential pharmaceutical compound for its possible biological activity. The ethylamino group and the complex structure of the molecule may contribute to its interaction with biological targets, making it a candidate for further research and development in the pharmaceutical field.
Used in Chemical Research:
This complex organic compound is also used in chemical research for studying the properties and reactions of molecules with intricate structures. Its unique features, such as the conjugated double bonds and the naphtho[2,1-b]furan ring system, may provide insights into the behavior of similar compounds and contribute to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 38129-09-8 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 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38129-09:
(7*3)+(6*8)+(5*1)+(4*2)+(3*9)+(2*0)+(1*9)=118
118 % 10 = 8
So 38129-09-8 is a valid CAS Registry Number.
38129-09-8Relevant academic research and scientific papers
McCarthy,Moore,Wysong,Aldrich
, p. 1272 - 1276 (1977)
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.
