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2-(2,5-Dimethyl-phenyl)-butyronitrile is an organic compound characterized by its molecular formula C12H15N. It features a butyronitrile group (a four-carbon chain with a nitrile group at the end) and a 2,5-dimethylphenyl group (a benzene ring with two methyl groups at the 2nd and 5th positions). This chemical is known for its aromatic characteristics due to the presence of the phenyl ring and is often used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a colorless to pale yellow liquid at room temperature and is insoluble in water but soluble in organic solvents. The compound is also recognized for its potential applications in the production of dyes and other specialty chemicals, highlighting its versatility in the chemical industry.

16213-87-9

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16213-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16213-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,1 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16213-87:
(7*1)+(6*6)+(5*2)+(4*1)+(3*3)+(2*8)+(1*7)=89
89 % 10 = 9
So 16213-87-9 is a valid CAS Registry Number.

16213-87-9Downstream Products

16213-87-9Relevant academic research and scientific papers

Synthesis of poly(methylphenyl)acetonitriles by the aryne reaction

Waggenspack,Tran,Taylor,Yeung,Morgan,Deshmukh,Khanapure,Biehl

, p. 765 - 768 (2007/10/02)

Several 2-(arylmethyl) derivatives of 3,6-dimethyl- and 3,4,5,6-tetramethylbenzonitriles have been prepared in good yields most likely by a tandem addition-rearrangement reaction of the appropriate bromoarene and arylacetonitrile under aryne-forming conditions. Additionally, several 2-aryl-2-(1,4-dimethyl-2-naphthyl)acetonitriles were obtained by the usual aryne mechanism from the reaction of 2-bromo-1,4-dimethylnaphthalene and arylacetonitriles with lithium tetramethylpiperidide.

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