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β-Phenylhydrazopropionitrile, also known as β-Phenylhydrazopropensaeuremethylester, is an organic compound with the chemical formula C9H8N2. It is a derivative of propionitrile, featuring a phenylhydrazone group attached to the β-carbon. β-Phenylhydrazopropensaeuremethylester is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is synthesized through the reaction of benzoyl chloride with propionitrile in the presence of a base, such as sodium hydroxide. β-Phenylhydrazopropionitrile is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Due to its reactivity and potential applications, it is an important compound in the field of organic chemistry and chemical engineering.

49597-10-6

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49597-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49597-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,9 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 49597-10:
(7*4)+(6*9)+(5*5)+(4*9)+(3*7)+(2*1)+(1*0)=166
166 % 10 = 6
So 49597-10-6 is a valid CAS Registry Number.

49597-10-6Downstream Products

49597-10-6Relevant articles and documents

Organocatalytic Hantzsch Type Reaction Using Aryl Hydrazines, Propiolic Acid Esters and Enals: Enantioselective Synthesis of Paroxetine

Chen, Lu,Zhang, Zhi,Zu, Liansuo

, p. 5385 - 5390 (2020)

Aryl hydrazines, propiolic acid esters and enals serve as a viable substrate combination for an organocatalytic enantioselective Hantzsch type reaction. The method converts readily available starting materials into important chiral heterocycles with good to excellent yields and enantioselectivities, and has addressed the longstanding scope limitation of the classic Hantzsch reaction in the asymmetric synthesis of 2,6-unsubstituted hydropyridines. The synthetic utility has been demonstrated by the concise enantioselective synthesis of paroxetine. (Figure presented.).

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