The chemical in question is a complex organic molecule with the name "7,11-Methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one, 12b-(acetyloxy)-12-(benzoyloxy)-1,2a,3,4,4a,6,9,10,11,12,12a,12b-dodecahydro-11-hydroxy-6-methoxy-4a,8,13,13-tetramethyl-4,9-bis[(triethyl silyl)oxy]-, [2aR-(2aa,4b,4ab,6b,9a,11a,12a,12aa,12ba)]-". 7,11-Methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one, 12b-(acetyloxy)-12-(benzoyloxy)-1,2a,3,4,4a,6,9,10,11,12,12a,12b-dod ecahydro-11-hydroxy-6-methoxy-4a,8,13,13-tetramethyl-4,9-bis[(triethyl silyl)oxy]-, [2aR-(2aa,4b,4ab,6b,9a,11a,12a,12aa,12ba)]- is characterized by a cyclodeca[3,4]benz[1,2-b]oxet-5-one core structure, which is a type of cyclic ketone. It features a dodecahedral carbon skeleton with various functional groups attached, including acetyloxy and benzoyloxy groups at the 12b and 12 positions, respectively. The molecule also contains a hydroxy group at the 11 position and a methoxy group at the 6 position. Additionally, it has two triethyl silyl ether groups at the 4 and 9 positions, which are commonly used as protecting groups in organic synthesis. The stereochemistry of the molecule is defined by the presence of multiple chiral centers, as indicated by the [2aR-(2aa,4b,4ab,6b,9a,11a,12a,12aa,12ba)]- notation. This complex structure suggests that the compound may have potential applications in advanced chemical research or pharmaceutical development, given its intricate arrangement of functional groups and stereochemistry.
The CAS Registry Mumber 183133-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,1,3 and 3 respectively; the second part has 2 digits, 9 and 8 respectively. Calculate Digit Verification of CAS Registry Number 183133-98: (8*1)+(7*8)+(6*3)+(5*1)+(4*3)+(3*3)+(2*9)+(1*8)=134 134 % 10 = 4 So 183133-98-4 is a valid CAS Registry Number.
183133-98-4Relevant academic research and scientific papers
PROCESS FOR THE PREPARATION CABAZITAXEL
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, (2014/03/24)
The present invention discloses a process for the preparation of 4-acetoxy-2α-benzoyloxy-5β,20-epoxy-1-hydroxy-7β,10β-dimethoxy-9-oxotax-11-en-13α-yl(2R,3S)-3-tert-butoxycarbonylamino-2-hydroxy-3-phenyl-propionate Cabazitaxel (I).
PROCESSES FOR THE PREPARATION OF CABAZITAXEL INVOLVING C(7) -OH AND C(13) -OH SILYLATION OR JUST C(7) -OH SILYLATION
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, (2013/05/23)
Disclosed are processes towards Cabazitaxel (I) starting from 10-Deacetylbaccatin (III) that involve steps of either 7-OH monosilylation (passing through formula V) or 7,13-disilylation (passing through formulae XI, XII). Isopropanol Solvates of Cabazitaxel and processes to make this are also described.
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Get Best Price for183133-98-47,11-Methano-5H-cyclodeca[3,4]benz[1,2-b]oxet-5-one, 12b-(acetyloxy)-12-(benzoyloxy)-1,2a,3,4,4a,6,9,10,11,12,12a,12b-dod ecahydro-11-hydroxy-6-methoxy-4a,8,13,13-tetramethyl-4,9-bis[(triethyl silyl)oxy]-, [2aR-(2aa,4b,4ab,6b,9a,11a,12a,12aa,12ba)]-
