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2-(4-aminophenyl)-4-methylpyridine is an organic compound with the molecular formula C12H12N2. It is a derivative of pyridine, featuring a pyridine ring with a methyl group at the 4-position and a phenyl ring attached at the 2-position, which is further substituted with an amino group at the 4-position. 2-(4-aminophenyl)-4-methylpyridine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and drugs. Its chemical structure endows it with unique reactivity and properties, making it a valuable building block in organic chemistry.

18471-74-4

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18471-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18471-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,7 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18471-74:
(7*1)+(6*8)+(5*4)+(4*7)+(3*1)+(2*7)+(1*4)=124
124 % 10 = 4
So 18471-74-4 is a valid CAS Registry Number.

18471-74-4Downstream Products

18471-74-4Relevant academic research and scientific papers

2-Pyridyl and 3-pyridylzinc bromides: direct preparation and coupling reaction

Kim, Seung-Hoi,Rieke, Reuben D.

scheme or table, p. 3135 - 3146 (2010/06/13)

A facile synthetic approach to the direct preparation of 2-pyridyl and 3-pyridylzinc bromides has been demonstrated using Rieke zinc with 2-bromopyridine and 3-bromopyridine, respectively. A variety of different electrophiles have been coupled with the resulting organozinc reagents to give the corresponding cross-coupling products in moderate to good yields.

Coupling reactions with haloaromatic amines and alcohols for a practical synthetic route to 2-substituted aminophenyl and hydroxyphenyl pyridines

Kim, Seung-Hoi,Rieke, Reuben D.

supporting information; experimental part, p. 6985 - 6988 (2010/02/27)

A practical synthetic route to 2-substituted aminophenyl and hydroxyphenyl pyridines has been developed. It has been accomplished by the cross-coupling reactions of readily available 2-pyridylzinc bromides with haloaromatic amines and alcohols under mild

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