3661-73-2 Usage
Uses
Used in Pharmaceutical Industry:
Benzamide, 4-ethenyl(9CI) serves as a crucial building block in the synthesis of a variety of pharmaceuticals and organic compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, Benzamide, 4-ethenyl(9CI) is used as a versatile intermediate for creating a range of organic compounds. Its reactivity and functional groups make it a valuable component in the production of specialty chemicals.
Used in Antifungal Applications:
Due to its antifungal properties, Benzamide, 4-ethenyl(9CI) can be utilized in the development of antifungal agents. This can be particularly beneficial in treating various fungal infections and controlling the growth of fungi in different settings.
Used in Anti-inflammatory Applications:
Benzamide, 4-ethenyl(9CI) also exhibits anti-inflammatory properties, making it a potential candidate for the development of anti-inflammatory drugs. This can aid in the management of inflammation-related conditions and provide relief to patients suffering from such ailments.
It is important to handle Benzamide, 4-ethenyl(9CI) with care, as it may be harmful if ingested, inhaled, or exposed to the skin. Proper safety measures should be taken during its use to minimize any potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 3661-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3661-73:
(6*3)+(5*6)+(4*6)+(3*1)+(2*7)+(1*3)=92
92 % 10 = 2
So 3661-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO/c1-2-7-3-5-8(6-4-7)9(10)11/h2-6H,1H2,(H2,10,11)
3661-73-2Relevant articles and documents
Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Vinyl Acetate in Dimethyl Isosorbide as a Sustainable Solvent
Su, Mincong,Huang, Xia,Lei, Chuanhu,Jin, Jian
supporting information, p. 354 - 358 (2022/01/15)
A nickel-catalyzed reductive cross-coupling has been achieved using (hetero)aryl bromides and vinyl acetate as the coupling partners. This mild, applicable method provides a reliable access to a variety of vinyl arenes, heteroarenes, and benzoheterocycles, which should expand the chemical space of precursors to fine chemicals and polymers. Importantly, a sustainable solvent, dimethyl isosorbide, is used, making this protocol more attractive from the point of view of green chemistry.
A general and efficient heterogeneous gold-catalyzed hydration of nitriles in neat water under mild atmospheric conditions
Liu, Yong-Mei,He, Lin,Wang, Miao-Miao,Cao, Yong,He, He-Yong,Fan, Kang-Nian
scheme or table, p. 1392 - 1396 (2012/10/07)
Mild, efficient and general: Titania decorated with nanometer-sized gold particles acts as an efficient catalyst for the selective hydration of a wide range of chemically diverse nitriles into valuable amides in neutral water, under mild atmospheric conditions (see image). The process shows promise for a facile and direct one-pot synthesis of ?μ-caprolactam, an industrially important molecule, starting from 6-aminocapronitrile. Copyright
Formation of Carbon-Carbon Bond on Solid Support: Application of the Stille Reaction
Deshpande, Milind S.
, p. 5613 - 5614 (2007/10/02)
Vinyl/Aryl stannanes couple smoothly with polymer bound aryl iodides.The cross-coupled products are obtained in excellent yield and purity after cleavage from the solid support.