1219741-94-2 Usage
Uses
Used in Organic Synthesis:
2-(4-cyclopropylphenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its unique reactivity makes it a valuable component in creating complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(4-cyclopropylphenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane is utilized as a key intermediate in the preparation of various pharmaceuticals. Its role in the synthesis of bioactive compounds contributes to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
2-(4-cyclopropylphenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane is also employed in the agrochemical industry, where it serves as a building block for the synthesis of agrochemicals. Its application in this field aids in the development of effective pesticides and other agricultural chemicals.
Used in Functional Materials:
2-(4-cyclopropylphenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane is used in the preparation of functional materials, where its unique properties contribute to the creation of materials with specific characteristics for various applications, such as in electronics, energy storage, and other advanced technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 1219741-94-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,7,4 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1219741-94:
(9*1)+(8*2)+(7*1)+(6*9)+(5*7)+(4*4)+(3*1)+(2*9)+(1*4)=162
162 % 10 = 2
So 1219741-94-2 is a valid CAS Registry Number.
1219741-94-2Relevant articles and documents
Reductive Cyclopropanations Catalyzed by Dinuclear Nickel Complexes
Zhou, You-Yun,Uyeda, Christopher
supporting information, p. 3171 - 3175 (2016/03/12)
Dinuclear Ni complexes supported by naphthyridine-diimine (NDI) ligands catalyze the reductive cyclopropanation of alkenes with CH2Cl2 as the methylene source. The use of mild terminal reductants (Zn or Et2Zn) confers significant functional-group tolerance, and the catalyst accommodates structurally and electronically diverse alkenes. Mononickel catalysts bearing related N chelates afford comparatively low cyclopropane yields (≤20 %). These results constitute an entry into catalytic carbene transformations from oxidized methylene precursors.
