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2-(4-Carboxyphenyl)-1,3,2-dioxaborinane is a boronic acid derivative with the molecular formula C10H11BO4. It features a dioxaborinane ring structure and contains a carboxyphenyl group and a boron atom. This chemical compound is known for its potential applications in organic synthesis and medicinal chemistry, particularly in the development of new pharmaceuticals and agrochemicals. The versatile nature of its molecular structure allows it to be a valuable building block for synthesizing various functionalized compounds, and its boron moiety enables participation in unique chemical reactions, making it a useful tool for creating complex organic molecules.

126747-13-5

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126747-13-5 Usage

Uses

Used in Organic Synthesis:
2-(4-CARBOXYPHENYL)-1,3,2-DIOXABORINANE is used as a building block for the synthesis of various functionalized compounds due to its versatile molecular structure and the presence of a carboxyphenyl group and boron atom.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2-(4-CARBOXYPHENYL)-1,3,2-DIOXABORINANE is used as a key intermediate in the development of new drugs. Its unique chemical properties and reactivity make it a valuable component in the synthesis of bioactive molecules with potential therapeutic applications.
Used in Agrochemical Development:
2-(4-CARBOXYPHENYL)-1,3,2-DIOXABORINANE is also utilized in the agrochemical industry for the creation of new pesticides and other crop protection agents. Its ability to participate in unique chemical reactions contributes to the development of innovative and effective agrochemical products.
Used in the Creation of Complex Organic Molecules:
2-(4-CARBOXYPHENYL)-1,3,2-DIOXABORINANE is used as a valuable tool in the synthesis of complex organic molecules. Its boron moiety allows it to engage in unique chemical reactions, facilitating the construction of intricate molecular structures with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 126747-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,4 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126747-13:
(8*1)+(7*2)+(6*6)+(5*7)+(4*4)+(3*7)+(2*1)+(1*3)=135
135 % 10 = 5
So 126747-13-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BO4/c12-10(13)8-2-4-9(5-3-8)11-14-6-1-7-15-11/h2-5H,1,6-7H2,(H,12,13)

126747-13-5SDS

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 4-(1,3,2-dioxaborinan-2-yl)benzoic acid

1.2 Other means of identification

Product number -
Other names 2-(4-carboxyphenyl)-1,3,2-dioxaborinane

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:126747-13-5 SDS

126747-13-5Relevant academic research and scientific papers

NOVEL BEXAROTENE ANALOGS

-

Page/Page column 22-23, (2011/09/19)

The present invention relates to analogs of bexarotene and methods of use thereof.

N-acylsulfonamide apoptosis promoters

-

, (2008/06/13)

N-Benzoyl arylsulfonamides having the formula are BCL-Xl inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-Xl inhibiting compositions and methods of promoting apoptosis in a mammal.

N-Acylsulfonamide apoptosis promoters

-

, (2008/06/13)

N-Benzoyl arylsulfonamides having the formula Are BCL-X1 inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-X1 inhibiting compositions and methods of promoting apoptosis in a mammal.

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