164526-16-3 Usage
Uses
Used in Pharmaceutical Research:
(7-AMINO-2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-(2-CHLORO-PHENYL)-METHANONE is used as a compound of interest for its potential development into pharmaceuticals. The presence of the benzo[1,4]dioxin ring indicates possible biological activities that could be harnessed for therapeutic purposes.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (7-AMINO-2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-(2-CHLORO-PHENYL)-METHANONE is used as a starting point for the design and synthesis of new drugs. Its structural features may allow for modifications that could enhance its interaction with specific biological targets, potentially leading to the creation of novel medications.
Used in Drug Development:
(7-AMINO-2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-(2-CHLORO-PHENYL)-METHANONE is used as a candidate in drug development due to its complex structure and the potential for it to exhibit pharmacological effects. (7-AMINO-2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-(2-CHLORO-PHENYL)-METHANONE may undergo further chemical modifications to optimize its properties for specific medical applications.
Used in Chemical Synthesis:
In the chemical synthesis industry, (7-AMINO-2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-(2-CHLORO-PHENYL)-METHANONE may be used as an intermediate or a building block in the synthesis of more complex molecules with specific applications in various fields, including materials science, agrochemicals, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 164526-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,5,2 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 164526-16:
(8*1)+(7*6)+(6*4)+(5*5)+(4*2)+(3*6)+(2*1)+(1*6)=133
133 % 10 = 3
So 164526-16-3 is a valid CAS Registry Number.
164526-16-3Relevant articles and documents
Synthesis of quinolin-2-ones by an intramolecular Knoevenagel condensation and by tandem Michael-Knoevenagel heterocyclization
Mochalov,Chasanov,Fedotov,Zefirov
experimental part, p. 1105 - 1121 (2012/03/26)
The synthesis of 2-(N-R-amino)- and 2-(N-vinylcarbonylamino)acylbenzenes has been carried out and their heterocyclization into quinolin-2-ones under the action of sodium ethylate has been studied.
SYNTHESIS OF 1,3-DIHYDRO-5(R)-7,8-ETHYLENEDIOXY-2H-1,4-BENZO-DIAZEPIN-2-ONES
Mochalov, S. S.,Kosynkin, D. V.,Yudin, I. D.,Atanov, V. N.,Shabarov, Yu. S.,Zefirov, N. S.
, p. 527 - 532 (2007/10/02)
1-Diazepin-2-ones have been prepared from 1,4-benzodioxane for the first time.
