857674-55-6 Usage
Description
(2,3,4,5-tetramethoxy-6-methyl)phenylboronic acid is a boronic acid derivative with the molecular formula C12H17BO6. It is a chemical compound that is commonly used as a building block in organic synthesis, particularly in the preparation of biologically active molecules and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
(2,3,4,5-tetramethoxy-6-methyl)phenylboronic acid is used as a building block for the synthesis of biologically active molecules and pharmaceuticals. Its unique structure and reactivity make it a valuable tool in the field of drug discovery.
Used in Advanced Materials Development:
(2,3,4,5-tetramethoxy-6-methyl)phenylboronic acid is used in the development of advanced materials, such as polymers. Its unique properties contribute to the creation of innovative materials with specific characteristics.
Used as a Catalyst in Organic Reactions:
(2,3,4,5-tetramethoxy-6-methyl)phenylboronic acid is used as a catalyst in various organic reactions. Its reactivity allows for the efficient and selective formation of desired products in chemical processes.
Used in Anticancer Research:
(2,3,4,5-tetramethoxy-6-methyl)phenylboronic acid has been studied for its potential anticancer properties. It is being investigated for its ability to target and inhibit the growth of cancer cells.
Used in Anti-inflammatory Research:
(2,3,4,5-tetramethoxy-6-methyl)phenylboronic acid has also been studied for its potential anti-inflammatory properties. It may be utilized in the development of treatments for inflammatory conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 857674-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,6,7 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 857674-55:
(8*8)+(7*5)+(6*7)+(5*6)+(4*7)+(3*4)+(2*5)+(1*5)=226
226 % 10 = 6
So 857674-55-6 is a valid CAS Registry Number.
857674-55-6Relevant articles and documents
A new fluorogenic transformation: Development of an optical probe for coenzyme Q
Tremblay, Matthew S.,Sames, Dalibor
, p. 2417 - 2420 (2007/10/03)
(Chemical Equation Presented) A new fluorogenic transformation based on a quinone reduction/lactonization sequence has been developed and evaluated as a tool for probing redox phenomena in a biochemical context. The probe presented herein is an irreversible redox probe and is reduced selectively by biologically relevant quinols such as ubiquinol but is inert to reduced nicotinamides (e.g., NADH). The ensuing cyclization is fast and quantitative and provides a measurable optical response.
