883989-49-9 Usage
Uses
Used in Organic Synthesis:
2,6-bis(oct-7-enyloxy)phenylboronic acid is used as a reagent for forming carbon-carbon bonds, particularly in the Suzuki coupling reaction. This reaction is a widely employed method for the synthesis of various organic compounds, making it a valuable tool in the field.
Used in Material Science:
2,6-bis(oct-7-enyloxy)phenylboronic acid is used as a building block in the development of new materials. Its unique structure allows for the creation of novel materials with potential applications in various industries.
Used in Pharmaceutical Industry:
2,6-bis(oct-7-enyloxy)phenylboronic acid is used as a precursor in the synthesis of drug molecules. Its potential application in the development of new pharmaceuticals highlights its importance in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 883989-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,9,8 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 883989-49:
(8*8)+(7*8)+(6*3)+(5*9)+(4*8)+(3*9)+(2*4)+(1*9)=259
259 % 10 = 9
So 883989-49-9 is a valid CAS Registry Number.
883989-49-9Relevant academic research and scientific papers
Polyols as templates for the synthesis of macrocycles from boronic acid building blocks
Luethje, Sonja,Bornholdt, Claudia,Luening, Ulrich
, p. 909 - 915 (2007/10/03)
By using a norbornane tetraol 2 as a template, a bis(alkenyl-oxy)- substituted boronic acid 5 was bound twice, and the resulting bis(boronic acid ester) 6 was cyclized by ring-closing metathesis. The product bimacrocycle 7, or its hydrogenated analogue 8,
