41970-77-8 Usage
Uses
Used in Pharmaceutical Industry:
(8E,14E,24E)-8-[(hex-5-en-1-yloxy)amino]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 complex structure and the presence of multiple functional groups that may interact with biological targets.
Used in Chemical Research:
In the field of chemical research, (8E,14E,24E)-8-{[(hex-5-en-1-yloxy)amino]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 can be used as a subject for studying the synthesis of complex organic molecules, as well as for investigating its potential reactivity and interactions with other molecules, which could lead to the discovery of new chemical reactions or applications.
Used in Material Science:
(8E,14E,24E)-8-[(hex-5-en-1-yloxy)amino]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's unique structure and functional groups may also find applications in material science, where it could be utilized in the development of new materials with specific properties, such as improved stability, reactivity, or biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 41970-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,7 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41970-77:
(7*4)+(6*1)+(5*9)+(4*7)+(3*0)+(2*7)+(1*7)=128
128 % 10 = 8
So 41970-77-8 is a valid CAS Registry Number.
41970-77-8Relevant academic research and scientific papers
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.
