132047-94-0 Usage
Description
(E)-6-HYDROXY-1-HEXENYLBORONIC ACID is a chemical compound characterized by the presence of a boronic acid functional group. It is derived from 6-hydroxy-1-hexene and is widely recognized for its utility in organic synthesis. (E)-6-HYDROXY-1-HEXENYLBORONIC ACID is particularly noted for its role in the formation of carbon-carbon and carbon-heteroatom bonds, showcasing its versatility and reactivity in various chemical transformations.
Uses
Used in Pharmaceutical Industry:
(E)-6-HYDROXY-1-HEXENYLBORONIC ACID is used as a key reagent in the synthesis of various pharmaceuticals. Its ability to form carbon-carbon and carbon-heteroatom bonds makes it a valuable component in the development of new drugs with diverse structures and therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, (E)-6-HYDROXY-1-HEXENYLBORONIC ACID is utilized as an intermediate in the production of agrochemicals. Its role in creating essential carbon bonds contributes to the synthesis of compounds with pesticidal, herbicidal, and fungicidal properties, enhancing crop protection and yield.
Used in Material Science:
(E)-6-HYDROXY-1-HEXENYLBORONIC ACID is employed as a building block in the development of new materials. Its reactivity and ability to form different types of chemical bonds allow for the creation of materials with unique properties, such as improved strength, flexibility, or conductivity.
Used in Organic Synthesis:
(E)-6-HYDROXY-1-HEXENYLBORONIC ACID is used as a versatile reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its participation in a wide range of chemical transformations makes it a valuable tool for creating complex molecular structures and advancing the field of organic chemistry.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
A significant application of (E)-6-HYDROXY-1-HEXENYLBORONIC ACID lies in its role as a reagent in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for the synthesis of various pharmaceuticals, agrochemicals, and materials, highlighting the compound's importance in the development of these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 132047-94-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,4 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132047-94:
(8*1)+(7*3)+(6*2)+(5*0)+(4*4)+(3*7)+(2*9)+(1*4)=100
100 % 10 = 0
So 132047-94-0 is a valid CAS Registry Number.
132047-94-0Relevant articles and documents
Oxidation of hydroxyl-substituted organotrifluoroborates
Molander, Gary A.,Petrillo, Daniel E.
, p. 9634 - 9635 (2007/10/03)
Potassium- and tetra-n-butylammonium organotrifluoroborates containing hydroxyl groups have been prepared and oxidized using several common oxidants. Aryl-, alkenyl-, and alkyltrifluoroborates containing both primary and secondary hydroxyl groups were oxi
