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4-((N,N-Dimethylamino)methyl)phenylboronic acid pinacol ester HCl is a chemical compound derived from boronic acid, featuring a pinacol ester group and an N,N-dimethylaminomethyl substituent. 4-((N,N-Dimethylamino)methyl)phenylboronic acid pinacol ester HCl is known for its stability and increased solubility in both organic solvents and water due to its pinacol ester and HCl salt forms, respectively. Its versatile nature and capability to form strong carbon-carbon bonds make it an essential reagent in organic synthesis, particularly for the Suzuki-Miyaura cross-coupling reaction.

1073371-85-3

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1073371-85-3 Usage

Uses

Used in Pharmaceutical Industry:
4-((N,N-Dimethylamino)methyl)phenylboronic acid pinacol ester HCl is used as a reagent in the synthesis of complex organic molecules for various pharmaceutical applications. Its ability to form carbon-carbon bonds facilitates the creation of diverse drug candidates with potential therapeutic properties.
Used in Materials Science:
In the field of materials science, 4-((N,N-Dimethylamino)methyl)phenylboronic acid pinacol ester HCl is utilized as a key component in the development of novel materials with specific properties. Its role in forming carbon-carbon bonds contributes to the structural integrity and performance of these materials.
Used in Organic Synthesis:
4-((N,N-Dimethylamino)methyl)phenylboronic acid pinacol ester HCl is employed as a reagent in organic synthesis for the Suzuki-Miyaura cross-coupling reaction. This reaction is crucial for the formation of carbon-carbon bonds, allowing chemists to construct a wide range of organic compounds with specific functionalities and applications.
Used in Research and Development:
In research and development settings, 4-((N,N-Dimethylamino)methyl)phenylboronic acid pinacol ester HCl is used as a tool to explore new chemical reactions and mechanisms. Its unique properties and reactivity provide insights into the behavior of boronic acid derivatives and their potential applications in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1073371-85-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,7 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1073371-85:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*7)+(3*1)+(2*8)+(1*5)=143
143 % 10 = 3
So 1073371-85-3 is a valid CAS Registry Number.

1073371-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names dimethyl{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl}amine hydrochloride

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:1073371-85-3 SDS

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