1774-11-4 Usage
Description
5-(2-FURYL)-1,3-CYCLOHEXANEDIONE is an organic compound that serves as a key reactant in the synthesis of various complex organic molecules, particularly in the preparation of 12-aryl(hetaryl)-9-(2-furyl)-7,8,9,10,11,12-hexahydrobenzo[a]-acridin-11-ones. These synthesized compounds are characterized by the presence of two asymmetric carbon atoms at positions C9 and C12, which can be crucial for their chemical properties and potential applications.
Uses
Used in Pharmaceutical Synthesis:
5-(2-FURYL)-1,3-CYCLOHEXANEDIONE is used as a reactant in the synthesis of 12-aryl(hetaryl)-9-(2-furyl)-7,8,9,10,11,12-hexahydrobenzo[a]-acridin-11-ones, which are compounds of interest in pharmaceutical research. These synthesized compounds may possess unique biological activities and therapeutic potential, making them valuable for the development of new drugs.
Used in Organic Chemistry Research:
In the field of organic chemistry, 5-(2-FURYL)-1,3-CYCLOHEXANEDIONE can be utilized as a building block for the creation of novel organic molecules with diverse structures and functionalities. Its use in research can lead to the discovery of new chemical reactions and the development of innovative synthetic pathways.
Used in Material Science:
The unique structural features of 5-(2-FURYL)-1,3-CYCLOHEXANEDIONE and its derivatives may also find applications in material science. The synthesized compounds could be explored for their potential use in the development of new materials with specific properties, such as optoelectronic materials, sensors, or advanced polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 1774-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1774-11:
(6*1)+(5*7)+(4*7)+(3*4)+(2*1)+(1*1)=84
84 % 10 = 4
So 1774-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O3/c11-8-4-7(5-9(12)6-8)10-2-1-3-13-10/h1-3,7H,4-6H2
1774-11-4Relevant articles and documents
Synthesis of New 3-(Furan-2-yl)-Substituted Dibenzo-Diazepin-1-one Derivatives
Wang, Fang-Ming,Bao, Dan,Wang, Ming,Yin, Qing-Huan,Chen, Li-Zhuang,Han, Guang-Fan
, p. 1081 - 1085 (2016)
A new series of 3-(furan-2-yl) dibenzo-diazepin-1-one derivatives were synthesized by condensation of 5-(furan-2-yl)-1,3-cyclohexanedione, o-phenylenediamine, and aromatic aldehydes, in which in some of them existed two very close isomer compounds. All the compounds were characterized by IR, MS,1H NMR, and elemental analysis. Also presented were the crystal structures of 3a, 3b and 3e, which were obtained and determined by X-ray single-crystal diffraction.
PROCESS FOR THE PRODUCTION OF OPTICALLY ACTIVE CYCLIC ENAMINONE DERIVATIVES
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, (2008/06/13)
A process for the production of optically active cyclic enaminone derivatives characterized by aminating one of the carbonyl groups of a cyclic 1,3-diketone derivative having a symmetry plane to obtain an optically isomeric mixture of chiral cyclic enamin
