61599-79-9 Usage
Description
Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)-, also known as 6-Iodo-5-(1,3-benzodioxol-6-yl)-1,3-benzodioxol-2-one, is a chemical compound with the molecular formula C10H7IO4. It is a derivative of 1,3-benzodioxole with a substituent at the 6 position. Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is utilized in organic synthesis and pharmaceutical research as a building block for the preparation of various biologically active molecules and pharmaceutical products. Additionally, it has been studied for its potential pharmacological properties and therapeutic applications. However, due to its potential hazards and toxic effects, it is crucial to handle this chemical with caution and adhere to proper safety protocols.
Uses
Used in Organic Synthesis:
Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is used as a building block in organic synthesis for the creation of various biologically active molecules. Its unique structure allows for the development of new compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In pharmaceutical research, Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is utilized as a key component in the preparation of pharmaceutical products. Its properties make it a valuable asset in the development of new drugs and therapeutic agents.
Used in the Development of Biologically Active Molecules:
Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is also used in the development of biologically active molecules, which can have significant implications in medicine and healthcare. Its potential pharmacological properties and therapeutic applications are currently being explored, making it an important compound in the field of pharmaceuticals.
Used in Safety and Hazard Management:
Due to its potential hazards and toxic effects, Ethanone, 1-(6-iodo-1,3-benzodioxol-5-yl)is also used as a reference in safety and hazard management protocols. Understanding its properties and risks can help in the development of proper handling and storage procedures to ensure the safety of researchers and workers in the industry.
Check Digit Verification of cas no
The CAS Registry Mumber 61599-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,9 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61599-79:
(7*6)+(6*1)+(5*5)+(4*9)+(3*9)+(2*7)+(1*9)=159
159 % 10 = 9
So 61599-79-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H7IO3/c1-5(11)6-2-8-9(3-7(6)10)13-4-12-8/h2-3H,4H2,1H3
61599-79-9Relevant articles and documents
A Serendipitous One-Pot Cyanation/Hydrolysis/Enamide Formation: Direct Access to 3-Methyleneisoindolin-1-ones
Banik, Trisha,Kaliappan, Krishna P.
supporting information, p. 628 - 633 (2020/12/09)
A direct, one-pot conversion of 2’-haloacetophenones to 3-methyleneisoindolin-1-one scaffolds using CuCN as the sole reagent without the need for moisture-free or anaerobic conditions is reported. This serendipitously discovered transformation with a broa
Copper-Catalyzed Domino Synthesis of 2-Arylthiochromanones through Concomitant C-S Bond Formations Using Xanthate as Sulfur Source
Sangeetha, Subramani,Muthupandi, Pandi,Sekar, Govindasamy
supporting information, p. 6006 - 6009 (2016/01/09)
An efficient domino process for the synthesis of thioflavanones has been described using a copper catalyst without addition of any external ligand. A variety of thioflavanones have been synthesized from easily accessible 2′-iodochalcones or 2′-bromochalco
Pd-catalyzed tandem homocoupling-aldol-dehydration of ortho-acylphenyl iodides
Fu, Meiqin,Lin, Dongen,Deng, Yuanfu,Zhang, Xiao-Qi,Liu, Yanchu,Lai, Chunsong,Zeng, Wei
, p. 23595 - 23603 (2014/07/07)
A Pd-catalyzed cascade Ullmann coupling-aldol-dehydration reaction of ortho-acylphenyl iodides has been explored. This transformation provides a concise access to colchino analogues in moderate to good yields with wide functional group tolerance.
