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2-(o-tolylaminomethyl)phenylboronic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1373320-84-3

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1373320-84-3 Usage

General Description

2-(o-tolylaminomethyl)phenylboronic acid is a chemical compound with the molecular formula C13H15BNO2. It is a boronic acid derivative containing a phenyl and tolyl group, as well as an amino group. 2-(o-tolylaminomethyl)phenylboronic acid is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura cross-coupling reaction, a widely used method for forming carbon-carbon bonds. It is also utilized in the preparation of various pharmaceutical compounds, agrochemicals, and materials science applications. The unique structure and reactivity of 2-(o-tolylaminomethyl)phenylboronic acid make it a valuable tool in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1373320-84-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,3,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1373320-84:
(9*1)+(8*3)+(7*7)+(6*3)+(5*3)+(4*2)+(3*0)+(2*8)+(1*4)=143
143 % 10 = 3
So 1373320-84-3 is a valid CAS Registry Number.

1373320-84-3Downstream Products

1373320-84-3Relevant academic research and scientific papers

Imino- and aminomethylphenylboronic acids: Stabilizing effect of hydrogen bonds

Adamczyk-Wo?niak, Agnieszka,Cyrański, Micha? K.,Frczak, Beata T.,Lewandowska, Agnieszka,Madura, Izabela D.,Sporzyński, Andrzej

experimental part, p. 3761 - 3767 (2012/06/30)

ortho-Iminomethylphenylboronic acids were synthesized from the reaction of 2-formyl-phenylboronic acid with primary aromatic amines. Reduction of these compounds yielded the corresponding aminomethylphenylboronic acids. For both types of the compounds, th

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