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Z-1-cyano-2-methyl-3-phenylpropene is an organic compound with the molecular formula C12H11N. It is a conjugated diene, featuring a cyano group (-CN) at the 1-position, a methyl group (-CH3) at the 2-position, and a phenyl group (C6H5) at the 3-position. Z-1-cyano-2-methyl-3-phenylpropene is characterized by its geometric isomerism, with the Z-configuration indicating that the phenyl and cyano groups are on the same side of the double bond. It is a colorless to pale yellow liquid with a pungent odor and is used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is typically handled with care in a controlled environment.

81639-79-4

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81639-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81639-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,3 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81639-79:
(7*8)+(6*1)+(5*6)+(4*3)+(3*9)+(2*7)+(1*9)=154
154 % 10 = 4
So 81639-79-4 is a valid CAS Registry Number.

81639-79-4Relevant academic research and scientific papers

The Photochemistry of 1-Cyano-2-methyl-3-phenylpropene and Ring substituted Derivatives

Ferreira, Aurelio B. B.,Salisbury, Kingsley

, p. 25 - 30 (2007/10/02)

The E- and Z-isomers of 1-cyano-2-methyl-3-phenylpropene and ring-substituted derivatives of the E-isomer, are shown to fluoresce and undergo Z-E-isomerization and di-?-methane rearrangement on irradiation.The rate constants for these processes, obtained from fluorescence lifetimes and quantum yields, can be analysed in terms of an initial interaction between the two ? systems, facilitated by partial charge-transfer, followed by two diverging pathways, one, towards a diradicaloid species leading to cyclopropane formation, the other towards a 'zwitterionic' species and relaxation to the ground state and resulting in singlet state Z-E-isommerization.

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