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Boc-6-Amino-5-methylpyridine-3-boronic acid pinacol ester is a boronic acid derivative that is widely used in organic synthesis and medicinal chemistry. It features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility. Boc-6-Amino-5-methylpyridine-3-boronic acid pinacol ester is known for its ability to form stable complexes with biological molecules such as proteins and nucleic acids, making it a valuable building block for the creation of diverse organic molecules through Suzuki-Miyaura cross-coupling reactions.

1075249-37-4

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1075249-37-4 Usage

Uses

Used in Pharmaceutical Development:
Boc-6-Amino-5-methylpyridine-3-boronic acid pinacol ester is used as a key intermediate in the synthesis of pharmaceuticals for its ability to form stable complexes with biological targets, contributing to the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Synthesis:
In the agrochemical industry, Boc-6-Amino-5-methylpyridine-3-boronic acid pinacol ester is utilized as a building block for the creation of agrochemicals, such as pesticides and herbicides, due to its reactivity and potential to form complexes with biologically relevant targets in plants and pests.
Used in Organic Synthesis:
Boc-6-Amino-5-methylpyridine-3-boronic acid pinacol ester is employed as a versatile reagent in organic synthesis for the construction of complex organic molecules. Its boronic acid functionality allows for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds and the synthesis of a wide range of organic compounds.
Used in Research and Development:
In academic and industrial research settings, Boc-6-Amino-5-methylpyridine-3-boronic acid pinacol ester is used as a valuable tool for exploring new chemical reactions and developing innovative synthetic methods. Its unique properties and reactivity make it an important compound for advancing the frontiers of chemical science.

Check Digit Verification of cas no

The CAS Registry Mumber 1075249-37-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,5,2,4 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1075249-37:
(9*1)+(8*0)+(7*7)+(6*5)+(5*2)+(4*4)+(3*9)+(2*3)+(1*7)=154
154 % 10 = 4
So 1075249-37-4 is a valid CAS Registry Number.

1075249-37-4SDS

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 tert-Butyl 2-((3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)amino)acetate

1.2 Other means of identification

Product number -
Other names -

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:1075249-37-4 SDS

1075249-37-4Relevant academic research and scientific papers

COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF CANNABINOID RECEPTOR 1 ACTIVITY

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Page/Page column 31-32, (2008/12/08)

The invention provides compounds and pharmaceutical compositions, and methods for using such compounds to treat, ameliorate or prevent a condition associated with activity of cannabinoid receptor 1 (CB1).

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