935446-54-1 Usage
Chemical structure
A boron atom bonded to two oxygen atoms and a phenyl ring with an iodo and a methoxy group.
Type of compound
A chemical compound.
Usage
Commonly used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds.
Stability
Known for its stability and high reactivity.
Applications
Found applications in pharmaceutical and agrochemical industries, as well as academic research.
Structure
Contains a boron atom.
Versatility
A versatile building block for the creation of new materials and molecular designs.
Check Digit Verification of cas no
The CAS Registry Mumber 935446-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,4,4 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 935446-54:
(8*9)+(7*3)+(6*5)+(5*4)+(4*4)+(3*6)+(2*5)+(1*4)=191
191 % 10 = 1
So 935446-54-1 is a valid CAS Registry Number.
935446-54-1Relevant articles and documents
Ortho-Selective C-H Borylation of Aromatic Ethers with Pinacol-borane by Organo Rare-Earth Catalysts
Xue, Can,Luo, Yong,Teng, Huailong,Ma, Yuanhong,Nishiura, Masayoshi,Hou, Zhaomin
, p. 5017 - 5022 (2018/05/14)
The regioselective C-H borylation of aromatic ethers such as anisoles is of much interest and importance, but has remained a challenge to date. We report herein the catalytic ortho-selective C-H borylation of a wide range of aromatic ethers with pinacolborane (HBpin) by rare-earth metallocene complexes. This protocol offers an efficient and straightforward route for the synthesis of a variety of borylated aromatic ether derivatives. A proper metal/ligand combination for the rare-earth metal catalysts was found to be critically important to promote this transformation.
