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2,4-dimethyl-2-phenyl-valeronitrile is an organic compound with the chemical formula C14H17N. It is a derivative of valeronitrile, featuring a phenyl group attached to the second carbon and two methyl groups on the second and fourth carbons of the valeronitrile backbone. 2,4-dimethyl-2-phenyl-valeronitrile is characterized by its nitrile functional group (C≡N), which is present at the end of the carbon chain. It is a colorless liquid with a distinct aroma and is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound's properties, such as its boiling point, solubility, and stability, are influenced by the presence of the phenyl and methyl groups, making it a versatile building block in organic chemistry.

4355-51-5

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4355-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4355-51-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4355-51:
(6*4)+(5*3)+(4*5)+(3*5)+(2*5)+(1*1)=85
85 % 10 = 5
So 4355-51-5 is a valid CAS Registry Number.

4355-51-5Downstream Products

4355-51-5Relevant academic research and scientific papers

Synthesis of Tertiary Benzylic Nitriles via Nickel-Catalyzed Markovnikov Hydrocyanation of α-Substituted Styrenes

Xing, Yidan,Yu, Rongrong,Fang, Xianjie

, p. 1008 - 1012 (2020/02/04)

The Markovnikov hydrocyanation of α-substituted styrenes enables the synthesis of tertiary benzylic nitriles under nickel catalysis. The Lewis-acid-free transformation features an unprecedented functional groups tolerance, including the-OH and-NH2 groups. A broad range of tertiary benzylic nitriles were obtained in good to excellent yields. In addition, an asymmetric version of this reaction was preliminarily investigated.

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