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1257651-17-4

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1257651-17-4 Usage

Description

3-[2-(Boc-amino)acetamido]benzeneboronic acid pinacol ester, 97% is a boronic acid pinacol ester derivative featuring a Boc-protected amino group. This chemical compound serves as a valuable building block in the preparation of various biologically active molecules and pharmaceuticals. Its high purity of 97% makes it a high-quality product suitable for research and development processes. It is an essential tool in the creation of complex organic molecules, particularly in the pharmaceutical and agrochemical industries.

Uses

Used in Organic Synthesis:
3-[2-(Boc-amino)acetamido]benzeneboronic acid pinacol ester, 97% is used as a building block for the synthesis of biologically active molecules and pharmaceuticals. Its Boc-protected amino group allows for the creation of complex organic molecules with potential applications in the pharmaceutical and agrochemical industries.
Used in Suzuki-Miyaura Coupling Reactions:
3-[2-(Boc-amino)acetamido]benzeneboronic acid pinacol ester, 97% is used as a reagent in Suzuki-Miyaura coupling reactions, which are crucial for the formation of carbon-carbon bonds in organic synthesis. This reaction plays a significant role in the development of new chemical compounds and the modification of existing ones, contributing to advancements in various fields, including pharmaceuticals and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-[2-(Boc-amino)acetamido]benzeneboronic acid pinacol ester, 97% is used as a key intermediate for the synthesis of drug candidates. Its unique structure and reactivity enable the development of novel therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Industry:
3-[2-(Boc-amino)acetamido]benzeneboronic acid pinacol ester, 97% is also utilized in the agrochemical industry as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its application in this field contributes to the development of more effective and environmentally friendly solutions for crop protection and management.

Check Digit Verification of cas no

The CAS Registry Mumber 1257651-17-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,7,6,5 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1257651-17:
(9*1)+(8*2)+(7*5)+(6*7)+(5*6)+(4*5)+(3*1)+(2*1)+(1*7)=164
164 % 10 = 4
So 1257651-17-4 is a valid CAS Registry Number.

1257651-17-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H51709)  3-[2-(Boc-amino)acetamido]benzeneboronic acid pinacol ester, 97%   

  • 1257651-17-4

  • 1g

  • 699.0CNY

  • Detail
  • Alfa Aesar

  • (H51709)  3-[2-(Boc-amino)acetamido]benzeneboronic acid pinacol ester, 97%   

  • 1257651-17-4

  • 5g

  • 2744.0CNY

  • Detail

1257651-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[2-oxo-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilino]ethyl]carbamate

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:1257651-17-4 SDS

1257651-17-4Downstream Products

1257651-17-4Relevant articles and documents

Design, synthesis and evaluation of a boronic acid based artificial receptor for l-DOPA in aqueous media

Ueno, Haruna,Iwata, Takayuki,Koshiba, Nozomi,Takahashi, Daisuke,Toshima, Kazunobu

, p. 10403 - 10405 (2013)

Design and synthesis of a boronic acid based artificial receptor which selectively and effectively bound to a neurotransmitter, l-DOPA (1), in aqueous media. In addition, the synthetic receptor was found to effectively inhibit the DDC (l-DOPA decarboxylase) enzymatic reaction under physiological conditions.

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