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3-(2H-TETRAZOL-5-YL)-PHENYL-BORONIC ACID is an organoboron compound with the molecular formula C7H7BN4O2, featuring a tetrazol-5-yl substituent at the 3-position of the phenyl ring. It is a derivative of phenylboronic acid and is widely recognized for its role in organic synthesis, particularly in the Suzuki-Miyaura cross-coupling reaction for forming carbon-carbon bonds. This versatile chemical also holds promise in pharmaceuticals and materials science, establishing its significance in the realm of organic chemistry.

775351-30-9

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775351-30-9 Usage

Uses

Used in Organic Synthesis:
3-(2H-TETRAZOL-5-YL)-PHENYL-BORONIC ACID is used as a reagent for the Suzuki-Miyaura cross-coupling reaction, a method crucial for creating carbon-carbon bonds in organic chemistry. Its unique structure with the tetrazol-5-yl group enhances the reactivity and selectivity of the boronic acid, making it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 3-(2H-TETRAZOL-5-YL)-PHENYL-BORONIC ACID is utilized as a building block for the development of new drugs. Its ability to form stable carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction allows for the creation of complex molecular structures with potential therapeutic properties. 3-(2H-TETRAZOL-5-YL)-PHENYL-BORONIC ACID's versatility and reactivity make it a promising candidate for the design of innovative pharmaceutical agents.
Used in Materials Science:
3-(2H-TETRAZOL-5-YL)-PHENYL-BORONIC ACID also finds applications in materials science, where it can be employed to develop new materials with unique properties. Its ability to form stable bonds and its compatibility with various other chemical entities make it suitable for the synthesis of advanced materials with potential applications in various fields, such as electronics, optoelectronics, and nanotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 775351-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,5,3,5 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 775351-30:
(8*7)+(7*7)+(6*5)+(5*3)+(4*5)+(3*1)+(2*3)+(1*0)=179
179 % 10 = 9
So 775351-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BN4O2/c13-8(14)6-3-1-2-5(4-6)7-9-11-12-10-7/h1-4,13-14H,(H,9,10,11,12)

775351-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(2H-tetrazol-5-yl)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 3-tetrazolephenylboronic 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:775351-30-9 SDS

775351-30-9Relevant academic research and scientific papers

2-METHYLMORPHOLINE PYRIDO-, PYRAZO- AND PYRIMIDO-PYRIMIDINE DERIVATIVES AS MTOR INHIBITORS

-

Page/Page column 108-109, (2008/06/13)

There is provided a compound of Formula (I), or a pharmaceutically acceptable salt thereof. There are also provided processes for the manufacture of a compound of Formula (1), and the use of a compound of Formula (1) as a medicament and in the treatment of cancer

Microwave-assisted preparation of aryltetrazoleboronate esters

Schulz, Mark J.,Coats, Steven J.,Hlasta, Dennis J.

, p. 3265 - 3268 (2007/10/03)

(Chemical Equation Presented) The addition of azido trimethylsilane to arylnitrileboronate esters is shown to proceed rapidly in dimethoxyethane to give aryltetrazoleboronate esters in moderate to good yields, with dibutyltin oxide as catalyst.

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