15016-42-9 Usage
Description
2-VINYLPHENYLBORONIC ACID is an organic compound that serves as a versatile building block in various chemical reactions and synthesis processes. It is characterized by its boronic acid functional group and a vinyl group attached to a phenyl ring, which allows for a wide range of applications in different industries.
Uses
Used in Organic Synthesis:
2-VINYLPHENYLBORONIC ACID is used as a key intermediate for the synthesis of various organic compounds. Its unique structure enables it to participate in numerous chemical reactions, making it a valuable asset in the field of organic chemistry.
Used in Pharmaceutical Industry:
2-VINYLPHENYLBORONIC ACID is used as a building block for the development of new pharmaceutical compounds. Its reactivity and structural diversity allow for the creation of novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
2-VINYLPHENYLBORONIC ACID is used as a starting material for the synthesis of various agrochemicals, such as pesticides and herbicides. Its versatility in chemical reactions enables the development of new and effective products for agricultural use.
Used in Dyestuff Industry:
2-VINYLPHENYLBORONIC ACID is used as a raw material for the production of dyes and pigments. Its chemical properties allow for the creation of a wide range of colorants with different shades and properties.
Used in Suzuki Reaction:
2-VINYLPHENYLBORONIC ACID is used as a coupling partner in the Suzuki reaction, a widely employed method for the formation of carbon-carbon bonds. This reaction is particularly useful in the synthesis of complex organic molecules and the development of new materials.
Check Digit Verification of cas no
The CAS Registry Mumber 15016-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,1 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15016-42:
(7*1)+(6*5)+(5*0)+(4*1)+(3*6)+(2*4)+(1*2)=69
69 % 10 = 9
So 15016-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9BO2/c1-2-7-5-3-4-6-8(7)9(10)11/h2-6,10-11H,1H2
15016-42-9Relevant articles and documents
A Sequential Pd-AAA/Cross-Metathesis/Cope Rearrangement Strategy for the Stereoselective Synthesis of Chiral Butenolides
Aubert, Sidonie,Katsina, Tania,Arseniyadis, Stellios
, p. 2231 - 2235 (2019/03/29)
A practical and highly enantio- (up to 94:6 er) and diastereoselective (up to >20:1 dr) synthesis of I-butenolides bearing two adjacent stereogenic centers is reported featuring a sequential direct palladium-catalyzed asymmetric allylic alkylation/(E)-selective cross-metathesis/[3,3]-sigmatropic Cope rearrangement from readily available α-substituted (5H)-furan-2-ones.
Stereoselective Synthesis of Exocyclic Tetrasubstituted Vinyl Halides via Ru-Catalyzed Halotropic Cycloisomerization of 1,6-Haloenynes
Trost, Barry M.,Kalnmals, Christopher A.
supporting information, p. 2346 - 2349 (2017/05/12)
Herein, a ruthenium-catalyzed cycloisomerization that transforms 1,6-haloenynes into 5-membered carbo- and heterocycles that bear exocyclic, stereodefined, tetrasubstituted vinyl halides is reported. The reaction is insensitive to air and water, tolerates a variety of functional groups, and proceeds with good to excellent stereoselectivity and yield.
Bromo-boronolactonization of olefins
Falck,Bondlela,Venkataraman,Srinivas
, p. 7148 - 7150 (2007/10/03)
Exposure of a variety of mono- and disubstituted ortho-alkenylarylboronic acids to NBS in THF/H2O under neutral conditions affords bromo-boronolactones, in some instances, with exceptional regiocontrol. The adducts, analogous to those formed by carboxylic acids, are shown to be useful synthetic intermediates.