6044-73-1 Usage
Description
11-(3-fluorophenyl)-3,3-dimethyl-10-(phenylacetyl)-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one is a complex organic compound with a unique molecular structure. It belongs to the class of dibenzodiazepines, which are known for their diverse range of biological activities and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
11-(3-fluorophenyl)-3,3-dimethyl-10-(phenylacetyl)-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one is used as a pharmaceutical compound for its potential therapeutic effects. Its specific application reason is due to its structural similarity to other dibenzodiazepines that have been found to possess various pharmacological properties, such as anti-anxiety, anticonvulsant, and muscle relaxant activities.
Used in Chemical Research:
In the field of chemical research, 11-(3-fluorophenyl)-3,3-dimethyl-10-(phenylacetyl)-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one can be used as a starting material or intermediate for the synthesis of other complex organic molecules. Its unique structure and functional groups make it a valuable candidate for further chemical modifications and exploration of new compounds with potential applications in various industries.
Used in Organic Synthesis:
11-(3-fluorophenyl)-3,3-dimethyl-10-(phenylacetyl)-2,3,4,5,10,11-hexahydro-1H-dibenzo[b,e][1,4]diazepin-1-one is used as a synthetic intermediate for the production of various organic compounds. Its application reason is based on its structural complexity and the presence of multiple functional groups that can be further modified or reacted with other molecules to create new compounds with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6044-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6044-73:
(6*6)+(5*0)+(4*4)+(3*4)+(2*7)+(1*3)=81
81 % 10 = 1
So 6044-73-1 is a valid CAS Registry Number.
6044-73-1Relevant articles and documents
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Said,E.Z.,Tipping,A.E.
, p. 1399 - 1403 (1972)
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Total synthesis of celastrol, development of a platform to access celastroid natural products
Camelio, Andrew M.,Johnson, Trevor C.,Siegel, Dionicio
supporting information, p. 11864 - 11867 (2015/10/06)
Celastroid natural products, triterpenes, have been and continue to be investigated in clinical trials. Celastrol, and for that matter any member of the celastroid family, was prepared for the first time through chemical synthesis starting from 2,3-dimethylbutadiene. A triene cyclization precursor generated in 12 steps underwent a nonbiomimetic polyene cyclization mediated by ferric chloride to generate the generic celastroid pentacyclic core. In the cyclization, engagement of a tetrasubstituted olefin formed adjacent all carbon quaternary centers stereospecifically. With access to the carbocyclic core of the family of natural products, wilforic acid and wilforol A were prepared en route to racemic celastrol.
The Reaction of 1,2:3,4-Diepoxy-2,3-dimethylbutane with Nucleophiles
Farkas, Frederic,Wellauer, Thomas,Esser, Thomas,Sequin, Urs
, p. 1511 - 1519 (2007/10/02)
To find out whether the 1,4-addition to 1,2:3,4-diepoxides, which so far has been observed only once, is of a more general character, we investigated the reaction of a variety of O-, C-, N-, and S-nucleophiles with the model compound 1,2:3,4-diepoxy-2,3-dimethylbutane (Scheme 4).In several cases, 1,4-addition products could, indeed, be observed besides the expected 1,2-adducts (Table).
