1192107-39-3 Usage
Uses
Used in Organic Synthesis:
2,6-dimethyl-4-methoxymethylphenyl boronic acid is used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds, playing a crucial role in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-dimethyl-4-methoxymethylphenyl boronic acid is used as a key intermediate in the development of therapeutic agents, owing to its ability to facilitate the construction of complex organic molecules with potential medicinal properties.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 2,6-dimethyl-4-methoxymethylphenyl boronic acid is utilized as a building block for the synthesis of various agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Materials Science:
2,6-dimethyl-4-methoxymethylphenyl boronic acid is also used in materials science for the development of advanced materials, taking advantage of its versatile reactivity and functional groups to create novel materials with improved properties.
Used in Suzuki-Miyaura Cross-Coupling Reaction:
A significant application of 2,6-dimethyl-4-methoxymethylphenyl boronic acid is in the Suzuki-Miyaura cross-coupling reaction, a widely used method in organic chemistry for the formation of new carbon-carbon bonds, particularly in the synthesis of biologically active compounds and materials with specific functions.
Check Digit Verification of cas no
The CAS Registry Mumber 1192107-39-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,1,0 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1192107-39:
(9*1)+(8*1)+(7*9)+(6*2)+(5*1)+(4*0)+(3*7)+(2*3)+(1*9)=133
133 % 10 = 3
So 1192107-39-3 is a valid CAS Registry Number.
1192107-39-3Relevant academic research and scientific papers
Abundant lattice inclusion phenomenon with sterically hindered and inherently shape-selective tetraarylpyrenes
Moorthy, Jarugu Narasimha,Natarajan, Palani,Venugopalan, Paloth
supporting information; experimental part, p. 8566 - 8577 (2010/03/01)
(Figure Presented) Tetraarylpyrenes H1-H4 that typify molecular systems with orthogonal planes and lack hydrogen bonding functional groups were designed as new host systems with three distinct domains for guest inclusion. In particular, H2 and H4 hosts are found to include a variety of guest molecules. We have determined 42 crystal structures overall (i) to establish the importance of skeletal features of the hosts, (ii) to determine their adaptability in binding diverse guest molecules, and (iii) to delineate favored domains for location of guest molecules and preferred modes of association of the host systems. The unique features of H1-H4 are found to permit binding of aliphatic and aromatic guest species differently: the small-sized guest molecules such as CHCl3, (CH3)2S, etc. are found to be bound in the basin domain, whereas aliphatic and aromatic guests are found to be included in the channel/concave and trough regions, respectively. The crystal structure analyses reveal that as many as 20 out of 28 inclusion compounds of H2 are isostructural with one or more; we have identified 8 different crystal packing types with which each inclusion compound may be associated. The guest-binding potential of host H2 has been exploited to demonstrate the utility of these host systems in (i) the separation of regioisomeric methyl-substituted benzenes and mixtures of cis-trans isomers of decalin, perhydroisoquinoline, and cinnamonitrile, (ii) the stabilization of the keto-enol form of 1,3-diketones, and (iii) the conformational locking of flexible cycloalkanes.
