3306-60-3 Usage
Description
(7S)-7-(acetylamino)-2,3,10-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-1-yl acetate is a complex chemical compound with a unique structure, featuring an acetylamino group, three methoxy groups, and a benzo[a]heptalen backbone. As a synthetic organic molecule, it holds potential for pharmaceutical or biological applications due to its distinctive structural characteristics. The presence of the acetylamino and methoxy groups may endow the compound with specific chemical and biological properties, which warrant further investigation to explore its full potential and effects.
Uses
Used in Pharmaceutical Industry:
(7S)-7-(acetylamino)-2,3,10-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-1-yl acetate is used as a potential pharmaceutical agent for its unique structural features. (7S)-7-(acetylamino)-2,3,10-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-1-yl acetate's acetylamino and methoxy groups may contribute to its interaction with biological targets, making it a candidate for the development of new drugs or therapies.
Used in Chemical Research:
In the field of chemical research, (7S)-7-(acetylamino)-2,3,10-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-1-yl acetate serves as a subject of study to understand its chemical properties, reactivity, and potential applications in various chemical processes. Its complex structure may offer insights into the development of new synthetic methods or the creation of novel chemical compounds.
Used in Material Science:
(7S)-7-(acetylamino)-2,3,10-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-1-yl acetate may be utilized in material science for the development of new materials with specific properties. (7S)-7-(acetylamino)-2,3,10-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-1-yl acetate's structural elements could be exploited to create materials with tailored characteristics for various applications, such as in electronics, coatings, or advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 3306-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3306-60:
(6*3)+(5*3)+(4*0)+(3*6)+(2*6)+(1*0)=63
63 % 10 = 3
So 3306-60-3 is a valid CAS Registry Number.
3306-60-3Relevant articles and documents
METHODS AND USES OF COLCHICINE DERIVATIVES
-
Page/Page column 58, (2020/01/24)
Colchicine derivative(s), method(s) and use(s) thereof for treatment of inflammation. In certain embodiments, the colchicine derivative is a compound of Formula I: (I)
The efficacy of new colchicine derivatives and viability of the T-Lymphoblastoid cells in three-dimensional culture using 19F MRI and HPLC-UV ex vivo
Bartusik, Dorota,Tomanek, Boguslaw,Lattova, Erika,Perreault, Helene,Tuszynski, Jack,Fallone, Gino
experimental part, p. 193 - 201 (2010/03/24)
The paper describes ex vivo applications of colchicine derivatives for the treatment of human T-Lymphoblastoid (CEM) cells. Moreover, the role of the substitutions of ring A at C-1 and C-7 side chain of colchicine analogues was probed by the synthesis and examination of their effects on the three-dimensional (3-D) CEM cells' growth. The CEM cells were cultured in the hollow fiber bioreactor (HFB) device. We used 1H and 19F magnetic resonance imaging (MRI) to monitor changes in 3-D CEM cell culture. 19F MRI was used for visualization of the cellular uptake of new fluorine derivatives. Before and after treatment CEM cells profile was investigated with high performance liquid chromatography (HPLC-UV). Crown Copyright
