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3,5-diiodo-4-(methoxymethoxy)benzonitrile is an organic compound characterized by its chemical formula C10H7I2NO3. This molecule features a benzene ring with a nitrile group (-CN) attached to the 4-position, and two iodine atoms (I) at the 3 and 5 positions. Additionally, a methoxymethoxy group (-OCH2OCH3) is present at the 4-position, which is adjacent to the nitrile group. 3,5-diiodo-4-(methoxymethoxy)benzonitrile is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. The presence of the iodine atoms and the methoxymethoxy group makes it a versatile building block for various chemical reactions and transformations.

2888-56-4

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2888-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2888-56-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,8 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2888-56:
(6*2)+(5*8)+(4*8)+(3*8)+(2*5)+(1*6)=124
124 % 10 = 4
So 2888-56-4 is a valid CAS Registry Number.

2888-56-4Relevant academic research and scientific papers

Alkoxyboration: Ring-closing addition of B-O σ bonds across alkynes

Hirner, Joshua J.,Faizi, Darius J.,Blum, Suzanne A.

supporting information, p. 4740 - 4745 (2014/04/17)

For nearly 70 years, the addition of boron-X σ bonds to carbon-carbon multiple bonds has been employed in the preparation of organoboron reagents. However, the significantly higher strength of boron-oxygen bonds has thus far precluded their activation for addition, preventing a direct route to access a potentially valuable class of oxygen-containing organoboron reagents for divergent synthesis. We herein report the realization of an alkoxyboration reaction, the addition of boron-oxygen σ bonds to alkynes. Functionalized O-heterocyclic boronic acid derivatives are produced using this transformation, which is mild and exhibits broad functional group compatibility. Our results demonstrate activation of this boron-O σ bond using a gold catalysis strategy that is fundamentally different from that used previously for other boron addition reactions.

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