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1167418-12-3

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1167418-12-3 Usage

General Description

1-(tert-butoxycarbonyl)-1H-indazol-5-ylboronic acid is a chemical compound with the molecular formula C15H16BNO4. It is often used as a building block in organic synthesis and as a reagent in various chemical reactions. The presence of both a boronic acid and a tert-butoxycarbonyl (Boc) protecting group in the molecule allows for versatile reactivity and potential for derivatization. 1-(tert-butoxycarbonyl)-1H-indazol-5-ylboronic acid has been studied for its potential applications in the synthesis of pharmaceuticals and other biologically active compounds. Additionally, its boronic acid functionality can enable it to participate in Suzuki coupling reactions and other types of cross-coupling chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1167418-12-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,7,4,1 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1167418-12:
(9*1)+(8*1)+(7*6)+(6*7)+(5*4)+(4*1)+(3*8)+(2*1)+(1*2)=153
153 % 10 = 3
So 1167418-12-3 is a valid CAS Registry Number.

1167418-12-3Downstream Products

1167418-12-3Relevant articles and documents

ARGININE METHYLTRANSFERASE INHIBITORS AND USES THEREOF

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Paragraph 0228-0229, (2014/09/30)

Described herein are compounds of Formula (I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds described herein are useful for inhibiting arginine methyltransferase activity. Methods of using the compounds for treating arginine methyltransferase-mediated disorders are also described.

Fluorination of boronic acids mediated by silver(I) Triflate

Furuya, Takeru,Ritter, Toblas

supporting information; experimental part, p. 2860 - 2863 (2009/12/05)

A regiospecific Ag-mediated fluorination reaction of aryl- and alkenylboronic acids and esters Is reported. The fluorination reaction uses commercially available reagents, does not require the addition of exogenous ligands, and can be performed on a multigram scale. This report discloses the first practical reaction sequence from arylboronic acid to aryl fluorides.

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