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2-((Diisopropylamino)methyl)phenylboronic acid is a specialty chemical compound characterized by the presence of boronic acid and phenyl groups, along with diisopropylamino and methyl groups. It is represented by the chemical formula C15H24BNO2. 2-((Diisopropylamino)methyl)phenylboronic acid is recognized for its versatility as a reactant in various chemical processes and is valued in the fields of organic synthesis, pharmaceuticals, and agrochemicals. Its utility as a chemical intermediate in medicinal chemistry is noteworthy, and it is considered a valuable asset in chemical research. However, due to its nature as an organic compound, it is essential to handle it with care in the laboratory to mitigate potential reactivity and health risks.

95753-26-7

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95753-26-7 Usage

Uses

Used in Organic Synthesis:
2-((Diisopropylamino)methyl)phenylboronic acid is used as a reactant in organic synthesis for its ability to participate in multiple chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-((Diisopropylamino)methyl)phenylboronic acid is used as a chemical intermediate, playing a crucial role in the development of new drugs and medicinal compounds.
Used in Agrochemicals:
2-((Diisopropylamino)methyl)phenylboronic acid is employed in the agrochemical sector, where it serves as a reactant in the synthesis of various agrochemical products, potentially contributing to the development of new pesticides or herbicides.
Used in Chemical Research:
2-((Diisopropylamino)methyl)phenylboronic acid is used as a research compound in chemical laboratories, where it aids in the exploration of new chemical pathways and the discovery of novel chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 95753-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,5 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95753-26:
(7*9)+(6*5)+(5*7)+(4*5)+(3*3)+(2*2)+(1*6)=167
167 % 10 = 7
So 95753-26-7 is a valid CAS Registry Number.

95753-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-((Diisopropylamino)methyl)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [2-[[di(propan-2-yl)amino]methyl]phenyl]boronic acid

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:95753-26-7 SDS

95753-26-7Relevant academic research and scientific papers

Synthesis and structure of potential Lewis acid-Lewis base bifunctional catalysts: 2-N,N-Diisopropylaminophenylboronate derivatives

Coghlan, Samuel W.,Giles, Richard L.,Howard, Judith A.K.,Patrick, Leonard G.F.,Probert, Michael R.,Smith, Gillian E.,Whiting, Andrew

, p. 4784 - 4793 (2007/10/03)

Directed ortho-metallation is used to introduce a boron function into N,N-diisopropylbenzamide, resulting in the formation of both borinate and boronate derivatives. N,N-Diisopropylbenzamide ortho-boronate pinacol ester can be reduced with sodium borohydr

BIFUNCTIONAL CATALYSTS

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Page 39, (2010/02/10)

Bifunctional Lewis acid - Lewis base catalyst of Formula (I): wherein O is a C2-60 optionally heteroatom containing substituted or unsubstituted hydrocarbon scaffold comprising pendant or integral bifunctional groups LA and LB wherein LA is a pendant or integral boron or silicon Lewis acid group and LB is a pendant or integral phosphorus or nitrogen Lewis base group and its salts, N-fanctionalised derivatives, dimer or oligomer thereof; processes for the preparation thereof; novel compounds and novel intermediates; a composition comprising a catalyst or compound of the invention; a kit comprising one or more catalysts; the use thereof as catalysts in selective transformations, kits therefor and processes for selective transformation reactions catalysed thereby; screening methods to identify catalysts for specific transformations; and kits therefor.

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