1423700-11-1 Usage
Description
Methyl 2-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is a complex organic chemical compound characterized by a phenyl group linked to a carbon atom, which is further connected to two oxygen atoms and another phenyl group. The molecule features a boron-containing group attached to a phenyl ring at the opposite end. methyl 2-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is widely recognized for its utility in organic synthesis and pharmaceutical applications.
Uses
Used in Organic Synthesis:
Methyl 2-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate serves as a valuable reagent in organic synthesis, particularly for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure allows for versatile reactions, making it a key component in creating a variety of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, this compound acts as an intermediate in the production of various drugs. Its role in the synthesis of medicinal compounds is crucial, as it can contribute to the development of new pharmaceuticals with improved therapeutic properties.
Used in Chemical Supply:
Methyl 2-phenyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is also available for purchase from chemical suppliers, making it accessible to researchers and manufacturers who require it for their specific applications in both research and commercial production.
Check Digit Verification of cas no
The CAS Registry Mumber 1423700-11-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,7,0 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1423700-11:
(9*1)+(8*4)+(7*2)+(6*3)+(5*7)+(4*0)+(3*0)+(2*1)+(1*1)=111
111 % 10 = 1
So 1423700-11-1 is a valid CAS Registry Number.
1423700-11-1Relevant articles and documents
Highly site-selective direct C-H bond functionalization of phenols with α-aryl-α-diazoacetates and diazooxindoles via gold catalysis
Yu, Zhunzhun,Ma, Ben,Chen, Mingjin,Wu, Hai-Hong,Liu, Lu,Zhang, Junliang
, p. 6904 - 6907 (2014/06/09)
An unprecedented direct C-H bond functionalization of unprotected phenols with α-aryl α-diazoacetates and diazooxindoles was developed. A tris(2,4-di-tert-butylphenyl) phosphite derived gold complex promoted the highly chemoselective and site-selective C-H bond functionalization of phenols and N-acylanilines with gold-carbene generated from the decomposition of diazo compounds, furnishing the corresponding products in moderate to excellent yields at rt. The salient features of this reaction include readily available starting materials, unprecedented C-H functionalization rather than X-H insertion, good substrate scope, mild conditions, high efficiency, and ease in further transformation. To the best of our knowledge, this is the first example of C-H functionalization of unprotected phenols with diazo compounds.
