125261-72-5 Usage
Uses
Used in Pharmaceutical Industry:
TRANS-2-BUTEN-2-YLBORONIC ACID is used as a reagent for the synthesis of complex organic molecules, particularly in the formation of carbon-carbon bonds through the Suzuki coupling reaction. This reaction is crucial for the development of new pharmaceutical compounds, facilitating the creation of diverse and effective medications.
Used in Advanced Material Production:
In the field of material science, TRANS-2-BUTEN-2-YLBORONIC ACID is utilized as a key component in the synthesis of advanced materials. Its ability to form carbon-carbon bonds is instrumental in the production of materials with unique properties, such as high strength, light weight, or specific electronic characteristics.
Used in Agrochemical Development:
TRANS-2-BUTEN-2-YLBORONIC ACID is employed as a building block in the development of new agrochemicals. Its role in organic synthesis allows for the creation of novel compounds with potential applications in agriculture, such as pesticides or herbicides, enhancing crop protection and yield.
Used in Natural Product Modification:
TRANS-2-BUTEN-2-YLBORONIC ACID is also used in the modification of natural products. TRANS-2-BUTEN-2-YLBORONIC ACID contributes to the alteration of naturally occurring substances to improve their properties or to create new derivatives with specific applications, such as in the fragrance, flavor, or cosmetic industries.
Check Digit Verification of cas no
The CAS Registry Mumber 125261-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,2,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125261-72:
(8*1)+(7*2)+(6*5)+(5*2)+(4*6)+(3*1)+(2*7)+(1*2)=105
105 % 10 = 5
So 125261-72-5 is a valid CAS Registry Number.
125261-72-5Relevant academic research and scientific papers
Gamsey, Soya,DeLaTorre, Kelly,Singaram, Bakthan
, p. 711 - 715 (2005)
Novel homochiral vinyloxazaborolidines have been synthesized and subsequently hydrogenated using palladium on carbon under ambient conditions to produce, after oxidation of the boronate group, enantiomerically enriched secondary alcohols (up to 20% ee). H
TRIAZOLE AGONISTS OF THE APJ RECEPTOR
-
Paragraph 01354, (2016/12/07)
Compounds of Formula I and Formula II, pharmaceutically acceptable salt thereof, stereoisomers of any of the foregoing, or mixtures thereof are agonists of the APJ Receptor and have use in treating cardiovascular and other conditions. Compounds of Formula I and Formula II have the following structures where the definitions of the variables are provided herein.
