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N-Tetradecylboronic acid, a boronic acid derivative with the chemical formula C14H29BO2, is a white crystalline solid possessing a molecular weight of 234.2 g/mol. It is widely recognized for its versatility in organic synthesis, pharmaceutical production, and as a component in the development of boronic acid-based sensors. Its potential antiviral, antibacterial, and anticancer properties further expand its applicability in the fields of chemistry, pharmaceuticals, and biotechnology.

100888-40-2

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100888-40-2 Usage

Uses

Used in Organic Synthesis:
N-Tetradecylboronic acid is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic compounds.
Used in Pharmaceutical Production:
As a precursor, N-Tetradecylboronic acid is utilized in the manufacturing process of diverse pharmaceuticals, playing a crucial role in the development of new medications.
Used in Agrochemicals:
N-Tetradecylboronic acid is employed in the production of agrochemicals, serving as a key intermediate in the synthesis of compounds that protect crops and enhance agricultural productivity.
Used in Sensor Development:
N-Tetradecylboronic acid is used as a component in the preparation of boronic acid-based sensors, which are designed for the detection of specific compounds, offering selective and sensitive analytical tools in various industries.
Used in Antiviral and Antibacterial Applications:
N-Tetradecylboronic acid has been studied for its potential antiviral and antibacterial properties, making it a candidate for the development of new treatments against viral and bacterial infections.
Used in Cancer Treatment Research:
N-Tetradecylboronic acid is investigated as a potential treatment for certain types of cancer, highlighting its potential role in oncology and the advancement of cancer therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 100888-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,8 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100888-40:
(8*1)+(7*0)+(6*0)+(5*8)+(4*8)+(3*8)+(2*4)+(1*0)=112
112 % 10 = 2
So 100888-40-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H31BO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17/h16-17H,2-14H2,1H3

100888-40-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L19966)  1-Tetradecylboronic acid   

  • 100888-40-2

  • 1g

  • 381.0CNY

  • Detail
  • Alfa Aesar

  • (L19966)  1-Tetradecylboronic acid   

  • 100888-40-2

  • 5g

  • 1362.0CNY

  • Detail
  • Alfa Aesar

  • (L19966)  1-Tetradecylboronic acid   

  • 100888-40-2

  • 25g

  • 5464.0CNY

  • Detail

100888-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name tetradecylboronic acid

1.2 Other means of identification

Product number -
Other names Tetradecylboronsaeure

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:100888-40-2 SDS

100888-40-2Downstream Products

100888-40-2Relevant academic research and scientific papers

Method to improve cold flow resistance of polymers

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, (2010/06/11)

A method for reducing the cold flow of a polymeric composition of matter by introducing polymer with the combination or reaction product of (i) an acetal or ketal of an alditol and (ii)(a) a hydrocarbylated boric acid, (b) an organoaluminum compound, or (c) both a hydrocarbylated boric acid and an organoaluminum compound.

Lipase Inhibitors

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Page/Page column 8-9, (2009/09/05)

The present invention relates to inhibitors of lipases, such as inhibitors of endothelial lipase, as well as pharmaceutical compositions thereof, and methods for using such inhibitors. The prototype of these inhibitors has lipophilic portion and an electrophilic site.

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