1345024-09-0 Usage
Boron-containing compound
2-(3,5-dimethoxy-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane contains a boron atom, which is a key feature of its chemical properties and reactivity.
Boronic acid derivative
The compound is a derivative of boronic acid, which gives it unique chemical properties and makes it useful for a variety of applications in organic synthesis and medicinal chemistry.
Bulky and highly sterically hindered structure
The compound has a large and bulky structure, which can make it difficult for it to react with other molecules. This property can be useful in certain applications, such as Suzuki-Miyaura cross-coupling reactions.
Used in Suzuki-Miyaura cross-coupling reactions
2-(3,5-dimethoxy-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane can be used as a coupling agent in Suzuki-Miyaura reactions, which are a type of organic reaction used to form carbon-carbon bonds.
Selective functionalization of aryl halides
The compound can be used as a reagent to selectively functionalize aryl halides, which are important intermediates in organic synthesis.
Incorporated into pharmaceutical intermediates
2-(3,5-dimethoxy-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane can be incorporated into various pharmaceutical intermediates, which are used to synthesize drugs.
Potential applications in agrochemicals and materials science
The unique boron chemistry of 2-(3,5-dimethoxy-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane makes it a potentially useful compound in the development of agrochemicals and materials science applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1345024-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,0,2 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1345024-09:
(9*1)+(8*3)+(7*4)+(6*5)+(5*0)+(4*2)+(3*4)+(2*0)+(1*9)=120
120 % 10 = 0
So 1345024-09-0 is a valid CAS Registry Number.
1345024-09-0Relevant articles and documents
Total Synthesis of Chaetoglobin A via Catalytic, Atroposelective Oxidative Phenol Coupling
Kang, Houng,Torruellas, Carilyn,Liu, Jinchu,Kozlowski, Marisa C.
, p. 5554 - 5558 (2018)
The first total synthesis of chaetoglobin A (1), which features a chiral axis between two identical highly oxygenated bicyclic cores, was successfully completed in 12 steps from 2,6-dimethoxytoluene. Vanadium-catalyzed oxidative phenol coupling, as a key
Total syntheses of (+)-pestaphthalide A and (-)-pestaphthalide B
Schwaben, Jonas,Cordes, Jens,Harms, Klaus,Koert, Ulrich
experimental part, p. 2929 - 2934 (2011/10/30)
Total syntheses of (+)-pestaphthalide A and (-)-pestaphthalide B were achieved. Key steps are an iridium-mediated meta-selective arylborylation, a Suzuki-coupling/Jacobsen-epoxidation sequence, a stereodivergent epoxide opening and an anionic cyclic carbonate/-lactone rearrangement. Georg Thieme Verlag Stuttgart - New York.
