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1025900-35-9

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1025900-35-9 Usage

Description

(4-((diisopropylamino)methyl)phenyl)boronic acid is a chemical compound that is commonly used in organic synthesis and medicinal chemistry. It contains a boronic acid group, which enables it to form stable reversible covalent bonds with diols and amines, making it a useful building block for the synthesis of pharmaceuticals and other biologically active molecules. The presence of a diisopropylamino group also makes it a potential candidate for the development of new drugs, as this group is commonly found in many pharmaceutical compounds for its ability to enhance the solubility and stability of the molecule. Additionally, the phenyl group in the compound provides a convenient handle for further functionalization and modification, allowing for the synthesis of a wide variety of derivatives with different chemical properties and biological activities.

Uses

Used in Pharmaceutical Industry:
(4-((diisopropylamino)methyl)phenyl)boronic acid is used as a building block for the synthesis of pharmaceuticals and other biologically active molecules due to its ability to form stable reversible covalent bonds with diols and amines.
Used in Medicinal Chemistry:
(4-((diisopropylamino)methyl)phenyl)boronic acid is used as a potential candidate for the development of new drugs, as the diisopropylamino group enhances the solubility and stability of the molecule.
Used in Organic Synthesis:
(4-((diisopropylamino)methyl)phenyl)boronic acid is used for the synthesis of a wide variety of derivatives with different chemical properties and biological activities, thanks to the phenyl group that provides a convenient handle for further functionalization and modification.

Check Digit Verification of cas no

The CAS Registry Mumber 1025900-35-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,9,0 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1025900-35:
(9*1)+(8*0)+(7*2)+(6*5)+(5*9)+(4*0)+(3*0)+(2*3)+(1*5)=109
109 % 10 = 9
So 1025900-35-9 is a valid CAS Registry Number.

1025900-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Boronic acid, B-?[4-?[[bis(1-?methylethyl)?amino]?methyl]?phenyl]?-

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:1025900-35-9 SDS

1025900-35-9Downstream Products

1025900-35-9Relevant articles and documents

Bronsted base-assisted boronic acid catalysis for the dehydrative intramolecular condensation of dicarboxylic acids

Sakakura, Akira,Ohkubo, Takuro,Yamashita, Risa,Akakura, Matsujiro,Ishihara, Kazuaki

supporting information; experimental part, p. 892 - 895 (2011/05/02)

Bronsted base-assisted boronic acid catalysis for the dehydrative self-condensation of carboxylic acids is described. Arylboronic acid bearing bulky (N,N-dialkylamino)methyl groups at the 2,6-positions can catalyze the intramolecular dehydrative condensation of di-and tetracarboxylic acids. This is the first successful method for the catalytic dehydrative self-condensation of carboxylic acids.(Figure Presented)

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