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3-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is a chemical compound with the molecular formula C15H17BO6NO4. It is a nitrobenzoic acid derivative that contains a boronic acid functional group. 3-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is characterized by its potential for versatile chemical reactions and applications in various fields.

1218791-11-7

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  • 3-NITRO-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOIC ACID

    Cas No: 1218791-11-7

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1218791-11-7 Usage

Uses

Used in Organic Synthesis:
3-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is used as a building block in organic synthesis for the production of various pharmaceuticals and bioactive molecules. Its unique structure allows for the creation of a wide range of compounds with diverse properties and applications.
Used in Pharmaceutical Research:
In Pharmaceutical Research, 3-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is used as a key intermediate in the synthesis of new drug candidates. Its reactivity and functional groups make it a valuable component in the development of innovative medications.
Used in Suzuki Coupling Reactions:
3-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is used as a reagent in Suzuki coupling reactions, which are cross-coupling processes that facilitate the formation of carbon-carbon bonds. This reaction is crucial for the synthesis of complex organic molecules, including those with potential pharmaceutical applications.
Used in the Formation of Heterocycles:
3-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is also utilized in the formation of heterocycles, which are organic compounds containing a ring of atoms with at least one heteroatom. Heterocycles are important structural motifs in many biologically active molecules and pharmaceuticals.
Used in Fluorescence-Based Sensing and Bioimaging Applications:
The boronic acid group in 3-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid has been found to have potential for use in fluorescence-based sensing and bioimaging applications. This makes it a valuable tool for detecting and visualizing specific biomolecules or cellular structures, contributing to advancements in diagnostics and therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 1218791-11-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,8,7,9 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1218791-11:
(9*1)+(8*2)+(7*1)+(6*8)+(5*7)+(4*9)+(3*1)+(2*1)+(1*1)=157
157 % 10 = 7
So 1218791-11-7 is a valid CAS Registry Number.

1218791-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Carboxy-2-nitrophenylboronic acid, pinacol ester

1.2 Other means of identification

Product number -
Other names 3-Nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic 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:1218791-11-7 SDS

1218791-11-7Upstream product

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