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1-(Ethoxycarbonyl)pyrrole-3-boronic acid, pinacol ester is a versatile chemical compound that is a pinacol ester derivative of pyrrole-3-boronic acid. Its ethoxycarbonyl group enhances its stability and reactivity in various organic synthesis reactions. 1-(Ethoxycarbonyl)pyrrole-3-boronic acid, pinacol ester is widely used as a building block in the preparation of pharmaceuticals, agrochemicals, and organic materials due to its boronic acid functional group, which allows it to participate in Suzuki-Miyaura cross-coupling reactions for the construction of carbon-carbon bonds.

1256360-06-1

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  • Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1-carboxylate

    Cas No: 1256360-06-1

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1256360-06-1 Usage

Uses

Used in Pharmaceutical Industry:
1-(Ethoxycarbonyl)pyrrole-3-boronic acid, pinacol ester is used as a key building block for the synthesis of various pharmaceutical compounds. Its reactivity and stability make it suitable for the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(Ethoxycarbonyl)pyrrole-3-boronic acid, pinacol ester is employed as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its ability to form carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions contributes to the creation of novel and effective agrochemicals.
Used in Organic Material Synthesis:
1-(Ethoxycarbonyl)pyrrole-3-boronic acid, pinacol ester is utilized as a versatile reagent in the synthesis of various organic materials, including polymers, dyes, and sensors. Its unique properties enable the development of innovative materials with enhanced performance and functionality.
Used in Organic Synthesis Research:
As a valuable tool in organic chemistry, 1-(Ethoxycarbonyl)pyrrole-3-boronic acid, pinacol ester is widely used in research for exploring new synthetic routes, developing novel reactions, and understanding the fundamental principles of organic synthesis. Its reactivity and stability make it an ideal candidate for studying various reaction mechanisms and optimizing reaction conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1256360-06-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,6 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1256360-06:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*6)+(3*0)+(2*0)+(1*6)=141
141 % 10 = 1
So 1256360-06-1 is a valid CAS Registry Number.

1256360-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Ethoxycarbonyl)pyrrole-3-boronic acid, pinacol ester

1.2 Other means of identification

Product number -
Other names ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrole-1-carboxylate

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:1256360-06-1 SDS

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