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α-Benzenesulfonyl-2-methoxy-ξ-cinnamonitrile is a complex organic chemical compound with the molecular formula C15H13NO3S. It is characterized by the presence of a benzene ring with a sulfonyl group (-SO2-) attached to it, a methoxy group (-OCH3) at the 2nd position, and a cinnamonitrile group (-CH=CH-CN) at the ξ position. α-benzenesulfonyl-2-methoxy-ξ-cinnamonitrile is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving benzene derivatives and is used as an intermediate in the production of certain drugs and pesticides. The compound's properties, such as its solubility and stability, make it a valuable component in the development of new chemical entities.

16612-29-6

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16612-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16612-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,1 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16612-29:
(7*1)+(6*6)+(5*6)+(4*1)+(3*2)+(2*2)+(1*9)=96
96 % 10 = 6
So 16612-29-6 is a valid CAS Registry Number.

16612-29-6Downstream Products

16612-29-6Relevant academic research and scientific papers

Organocatalytic Cascade Knoevenagel–Michael Addition Reactions: Direct Synthesis of Polysubstituted 2-Amino-4H-Chromene Derivatives

Jadhav, Sanjay N.,Patil, Seema P.,Sahoo, Dipti Prava,Rath, Dharitri,Parida, Kulamani,Rode, Chandrashekhar V.

, p. 2331 - 2351 (2020/02/25)

Abstract: In this report, we documented novel strategy for the synthesis of bioactive polysubstituted 2-amino-4H-chromine derivatives under a heterogeneous Al-MCM-41-LDH@APTES (ALAM) catalysis. A synthetic procedure is developed to prepare Al-MCM-41-LDH@APTES (ALAM) heterogeneous basic catalysts. Mesoporous Al-MCM-41 is functionalized by known grafting chemistry via layered double hydroxide (LDH) nanosheets and (3-aminopropyl)triethoxysilane (APTES) moiety as a basic organocatalyst. The resulting catalysts contain amino group functionality on the external surface as well as inside the layers and the basicity can be tuned by the loading of APTES. The samples were fully characterized by 29Si and 13C CP/MAS NMR, infrared absorption spectroscopy, TEM, XPS, EDX, TGA, XRD, CO2-TPD, N2 adsorption isotherms measurements, and they were successfully examined for the cascade type Knoevenagel–Michael addition reactions. The product yields associated with these substrates were optimized, and key reaction parameters affecting the yields were identified. The present catalytic method is simple and robust for diversity oriented synthesis which proceeds good to excellent yields without generating any hazards waste. The broad substrate scope, excellent functional group compatibility makes this protocol highly useful towards synthesis of polysubstituted α-cyanoacrylates, α-cyanoacrylonitriles and 2-amino-4H-chromenes with an electron-donating or electron-withdrawing group. We have also successfully established a flow reaction system, gram-scale synthesis as well as catalyst recyclability up to six catalytic cycles without appreciable loss of its activity. Graphic Abstract: [Figure not available: see fulltext.].

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