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1029654-17-8

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1029654-17-8 Usage

General Description

2,4,6-Trimethylpyridine-3-boronic acid is a boronic acid derivative of trimethylpyridine, a heterocyclic compound. It is commonly used in organic synthesis as a reagent for Suzuki-Miyaura cross-coupling reactions and other types of C-C bond formation. 2,4,6-TRIMETHYLPYRIDINE-3-BORONIC ACID is also used in the preparation of pharmaceutical intermediates and agrochemicals. Its boronic acid functionality allows for the formation of stable complexes with diols and other nucleophiles, making it a versatile tool in chemical synthesis. Additionally, 2,4,6-Trimethylpyridine-3-boronic acid has been investigated for its potential medicinal properties, particularly as an anti-cancer agent.

Check Digit Verification of cas no

The CAS Registry Mumber 1029654-17-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,9,6,5 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1029654-17:
(9*1)+(8*0)+(7*2)+(6*9)+(5*6)+(4*5)+(3*4)+(2*1)+(1*7)=148
148 % 10 = 8
So 1029654-17-8 is a valid CAS Registry Number.

1029654-17-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4,6-trimethylpyridin-3-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 2,4,6-Trimethylpyridine-3-boronic acid

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:1029654-17-8 SDS

1029654-17-8Downstream Products

1029654-17-8Relevant articles and documents

PYRAZOLOQUINOLINE DERIVATIVES

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Paragraph 0384, (2013/06/26)

A compound and/or pharmacologically acceptable salt thereof represented by the formula (I) has PDE9 inhibitory action, so that the intracerebral cGMP concentration is anticipated to be elevated. The PDE9 inhibitory action and the increase in cGMP lead to the improvement of learning and memory behaviors, and the compound (I) has applicability as a therapeutic agent for cognitive dysfunctions in Alzheimer's disease. wherein R1 is a hydrogen atom; R2 is an aromatic ring group, etc.; R3 is a hydrogen atom, etc; R4 is a hydrogen atom; R5 is an oxepanyl group, etc.; R6 is a hydrogen atom.

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