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(Z)-3-(4-Methoxy-phenyl)-2-methyl-acrylonitrile is a chemical compound with the molecular formula C12H11NO. It is an organic molecule characterized by a 2-methyl-acrylonitrile structure, which features a double bond between the second and third carbon atoms, with the third carbon being part of a nitrile group (C≡N). The compound also includes a 4-methoxy-phenyl group attached to the third carbon, which contributes a methoxy (-OCH3) substituent on the para position of the benzene ring. This molecule is known for its specific geometric isomerism, with the Z configuration indicating that the highest priority groups are on the same side of the double bond. It is often used in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

53587-73-8

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53587-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53587-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,8 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53587-73:
(7*5)+(6*3)+(5*5)+(4*8)+(3*7)+(2*7)+(1*3)=148
148 % 10 = 8
So 53587-73-8 is a valid CAS Registry Number.

53587-73-8Downstream Products

53587-73-8Relevant academic research and scientific papers

Synthesis of trisubstituted alkenes by reductive dehydroxylation of Baylis-Hillman adducts using polymethylhydrosiloxane (PMHS) and catalytic B(C6F5)3

Chandrasekhar,Chandrashekar,Vijeender,Reddy, M. Srinivasa

, p. 3475 - 3478 (2006)

B(C6F5)3 as a catalyst and polymethylhydrosiloxane as a hydride source have been employed for the reductive dehydroxylation of Baylis-Hillman adducts wherein the hydride adds in an SN2′ manner onto the unactivat

Palladium catalysed regio and stereoselective reduction of Baylis- Hillman coupling products derived allylic acetates

Pachamuthu, Kandaswamy,Vankar, Yashwant D.

, p. 5439 - 5442 (2007/10/03)

Acetates derived from a variety of the Baylis-Hillman products undergo reduction with HCOOH in the presence of Et3N, Pd(OAc)2, and dppe (or tri- isopropylphosphite) to yield the corresponding trisubstituted Z-olefins in good yields d

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