18410-39-4 Usage
Type of compound
Organic compound
Derivative
Naphthalene derivative
Molecular structure
Naphthalene ring with a trimethylsilyl group at the 2-position and a methoxy group at the 6-position
Usage in organic synthesis
Building block in the production of organic materials
Protecting group
Employed as a protecting group in organic chemistry reactions due to its steric and electronic properties
Reagent in synthesis
Can be used as a reagent in the synthesis of various organic compounds
Precursor to other derivatives
Acts as a precursor to other functionalized naphthalene derivatives
Applications
Has several applications in organic chemistry and materials science
Check Digit Verification of cas no
The CAS Registry Mumber 18410-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18410-39:
(7*1)+(6*8)+(5*4)+(4*1)+(3*0)+(2*3)+(1*9)=94
94 % 10 = 4
So 18410-39-4 is a valid CAS Registry Number.
18410-39-4Relevant articles and documents
Nickel-Catalyzed Alkoxy–Alkyl Interconversion with Alkylborane Reagents through C?O Bond Activation of Aryl and Enol Ethers
Guo, Lin,Liu, Xiangqian,Baumann, Christoph,Rueping, Magnus
supporting information, p. 15415 - 15419 (2016/12/03)
A nickel-catalyzed alkylation of polycyclic aromatic methyl ethers as well as methyl enol ethers with B-alkyl 9-BBN and trialkylborane reagents that involves the cleavage of stable C(sp2)?OMe bonds is described. The transformation has a wide substrate scope and good chemoselectivity profile while proceeding under mild reaction conditions; it provides a versatile way to form C(sp2)?C(sp3) bonds that does not suffer from β-hydride elimination. Furthermore, a selective and sequential alkylation process by cleavage of inert C?O bonds is presented to demonstrate the advantage of this method.
