1073338-99-4 Usage
Chemical structure
The compound contains a boron atom at the center with a 1,3,2-dioxaborolane ring system and a phenyl group with an iodine and methoxy substituent.
Reactivity
The compound is highly reactive due to the presence of a tetramethyl-substituted boron center, making it useful in cross-coupling reactions to form carbon-carbon bonds.
Substituents
The compound has a phenyl group with a 3-iodo and 5-methoxy substituent, which imparts unique properties and reactivity to the molecule.
Applications
The compound is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of pharmaceuticals and other organic compounds.
Versatility
The compound's reactivity and structural features make it valuable for the development of new chemical entities and drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 1073338-99-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,3 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1073338-99:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*3)+(3*8)+(2*9)+(1*9)=154
154 % 10 = 4
So 1073338-99-4 is a valid CAS Registry Number.
1073338-99-4Relevant articles and documents
BORONIC ACID COMPOSITIONS AND METHODS RELATED TO CANCER
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, (2011/04/13)
Disclosed are compounds and methods related to boronic acid derivatives of resveratrol. Certain of these derivatives have enhanced efficacy relative to resveratrol, function as irreversible modulators, and act at the Gl/S phase of the cell cycle.
