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898289-06-0

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898289-06-0 Usage

General Description

1-Methyl-1H-indole-4-boronic acid, pinacol ester, 97%, also known as 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole, is a chemical compound used in organic synthesis and pharmaceutical research. It is a boronic acid ester with a pinacol group attached to the boron atom, which makes it a useful reagent for Suzuki-Miyaura cross-coupling reactions. 1-METHYL-1H-INDOLE-4-BORONIC ACID, PINACOL ESTER 97%1-METHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDOLE is commonly used as a building block for drug discovery and development, as well as in the synthesis of various biologically active molecules. Its high purity level of 97% makes it a reliable and effective reagent for chemical and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 898289-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,2,8 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 898289-06:
(8*8)+(7*9)+(6*8)+(5*2)+(4*8)+(3*9)+(2*0)+(1*6)=250
250 % 10 = 0
So 898289-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H20BNO2/c1-14(2)15(3,4)19-16(18-14)12-7-6-8-13-11(12)9-10-17(13)5/h6-10H,1-5H3

898289-06-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

1.2 Other means of identification

Product number -
Other names 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:898289-06-0 SDS

898289-06-0Downstream Products

898289-06-0Relevant articles and documents

SUBSTITUTED TRIAZOLO QUINOXALINE DERIVATIVES

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Page/Page column 49; 56, (2020/02/14)

The present invention relates to compounds according to general formula (I) which act as modulators of the glucocorticoid receptor and can be used in the treatment and/or prophylaxis of disorders which are at least partially mediated by the glucocorticoid receptor.

METHODS OF MANUFACTURING OF BORON COMPOUND WITHOUT TRANSITION METALS

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Paragraph 0065; 0066; 0071; 0072; 0079, (2018/05/03)

The present invention refers to aryl boron compound number bath method relates to search, more particularly transition metal catalyst to a tank without the use of boron compounds number is given to the aryl organic halo [ceyn [ceyn] freight method are disclosed to boron. (by machine translation)

Rhodium-catalyzed borylation of aryl 2-pyridyl ethers through cleavage of the carbon-oxygen bond: Borylative removal of the directing group

Kinuta, Hirotaka,Tobisu, Mamoru,Chatani, Naoto

, p. 1593 - 1600 (2015/03/05)

The rhodium-catalyzed reaction of aryl 2-pyridyl ethers with a diboron reagent results in the formation of arylboronic acid derivatives via activation of the C(aryl)-O bonds. The straightforward synthesis of 1,2-disubstituted arenes was enabled through catalytic ortho C-H bond functionalization directed by the 2-pyridyloxy group followed by substitution of this group with a boryl group. Several control experiments revealed that the presence of a sp2 nitrogen atom at the 2-position of the substrate and the use of a boron-based reagent were crucial for the activation of the relatively inert C(aryl)-O bond of aryl 2-pyridyl ethers.

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