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Benzenemethanimine, a-(1,1-dimethylethyl)-2-methyl-, also known as 2-methyl-α-(1,1-dimethylethyl)benzenemethanimine or 2-methyl-α-tert-butylbenzenemethanimine, is an organic compound with the chemical formula C12H17N. It is a derivative of benzenemethanimine, featuring a tert-butyl group (1,1-dimethylethyl) and a methyl group attached to the benzene ring. Benzenemethanimine, a-(1,1-dimethylethyl)-2-methyl- is characterized by its amine functional group, which consists of a nitrogen atom bonded to a carbon atom in the benzene ring. It is a colorless to pale yellow liquid with a pungent odor and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is typically handled with care and stored under controlled conditions to prevent unwanted reactions.

16620-72-7

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16620-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16620-72-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,2 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16620-72:
(7*1)+(6*6)+(5*6)+(4*2)+(3*0)+(2*7)+(1*2)=97
97 % 10 = 7
So 16620-72-7 is a valid CAS Registry Number.

16620-72-7Relevant academic research and scientific papers

Iron-Catalyzed ortho C?H Arylation and Methylation of Pivalophenone N?H Imines

Xu, Wengang,Yoshikai, Naohiko

, p. 3049 - 3053 (2019/03/13)

Iron-catalyzed ortho C?H arylation and methylation reactions of pivalophenone N?H imines are reported. The pivaloyl N?H imine proved an excellent directing group for the arylation with diarylzinc reagents in the presence of an iron-diphosphine catalyst an

Cobalt-Catalyzed, N-H Imine-Directed Arene C-H Benzylation with Benzyl Phosphates

Laskar, Roshayed Ali,Yoshikai, Naohiko

, p. 13172 - 13178 (2019/09/10)

A cobalt-catalyzed ortho-C-H benzylation reaction of pivalophenone N-H imines with benzyl phosphates is reported. The reaction is promoted at room temperature by a ternary catalytic system comprising Co(acac)3, a pyridylphosphine ligand, and a Grignard reagent and tolerates a series of substituted pivalophenone imines and benzyl phosphates to afford various diarylmethane derivatives in moderate yields.

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