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2-tert-butoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a complex organic chemical compound characterized by a pyridine ring with a tert-butoxy group at the 2-position and a 1,3,2-dioxaborolane ring with four methyl groups attached to the boron atom at the 4-position. 2-tert-butoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine's unique structure endows it with potential applications in various fields, particularly in organic synthesis, ligand chemistry, and the development of functional materials and pharmaceuticals.

1256358-89-0

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1256358-89-0 Usage

Uses

Used in Organic Synthesis:
2-tert-butoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is used as a building block in organic synthesis for the creation of various functional materials and pharmaceutical compounds. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of complex organic molecules.
Used in Ligand Chemistry for Transition Metal Catalysis:
In the field of catalysis, 2-tert-butoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a ligand for transition metal catalysts. Its ability to coordinate with metal centers enhances the catalytic activity and selectivity in various chemical transformations, making it a valuable component in the development of efficient and sustainable catalytic processes.
Used in the Preparation of Functional Materials:
2-tert-butoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is also utilized in the preparation of functional materials due to its unique structural features. Its incorporation into materials can impart specific properties, such as improved stability, reactivity, or selectivity, which are desirable for various applications in material science.
Used in Pharmaceutical Compounds:
2-tert-butoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity can be leveraged to develop new drugs with improved therapeutic properties, such as enhanced potency, selectivity, or bioavailability.

Check Digit Verification of cas no

The CAS Registry Mumber 1256358-89-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1256358-89:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*8)+(2*8)+(1*9)=180
180 % 10 = 0
So 1256358-89-0 is a valid CAS Registry Number.

1256358-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-t-Butoxypyridine-4-boronic acid pinacol ester

1.2 Other means of identification

Product number -
Other names 2-[(2-methylpropan-2-yl)oxy]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

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:1256358-89-0 SDS

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