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4-Methoxy-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a chemical compound with the molecular formula C15H19BO3. It is an aldehyde derivative that contains a benzene ring with a methoxy group and a boron-containing side chain.

443776-90-7

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443776-90-7 Usage

Uses

Used in Organic Synthesis:
4-Methoxy-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is used as a reagent for the formation of carbon-carbon bonds through the Suzuki coupling reaction. It is a highly versatile and valuable synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and organic materials.
Used in Pharmaceutical Industry:
4-Methoxy-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is used as a synthetic intermediate for the development of new pharmaceuticals.
Used in Agrochemical Industry:
4-Methoxy-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is used as a synthetic intermediate for the development of new agrochemicals.
Used in Material Science:
4-Methoxy-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde has potential applications in the development of new materials, such as polymers and liquid crystals.

Check Digit Verification of cas no

The CAS Registry Mumber 443776-90-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,7,7 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 443776-90:
(8*4)+(7*4)+(6*3)+(5*7)+(4*7)+(3*6)+(2*9)+(1*0)=177
177 % 10 = 7
So 443776-90-7 is a valid CAS Registry Number.

443776-90-7Downstream Products

443776-90-7Relevant academic research and scientific papers

Synthesis of some new biheterocycles by a one-pot Suzuki-Miyaura coupling reaction

Deodhar, Mandar,Black, David Stc.,Shiu-Hin Chan, Daniel,Kumar, Naresh

, p. 1267 - 1274 (2010)

Halogenated indoles, benzofurans and flavones were subjected to a one-pot Suzuki-Miyaura coupling reaction to generate a series of new biheterocycles. The methodology may be readily adapted to the synthesis of a wide variety of substituted biheterocycles.

Strategic Design of Catalytic Lysine-Targeting Reversible Covalent BCR-ABL Inhibitors**

Anantharajan, Jothi,Baburajendran, Nithya,Foo, Klement,Joy, Joma K.,Keller, Thomas H.,Kwek, Perlyn Z.,Li, Rong,Liu, Boping,Poulsen, Anders,Quach, David,Retna, Priya,Tang, Guanghui,Tee, Doris H. Y.,Wee, John L. K.,Yang, Wan-Qi,Yao, Shao Q.,Zhang, Chong-Jing

supporting information, p. 17131 - 17137 (2021/06/28)

Targeted covalent inhibitors have re-emerged as validated drugs to overcome acquired resistance in cancer treatment. Herein, by using a carbonyl boronic acid (CBA) warhead, we report the structure-based design of BCR-ABL inhibitors via reversible covalent targeting of the catalytic lysine with improved potency against both wild-type and mutant ABL kinases, especially ABLT315I bearing the gatekeeper residue mutation. We show the evolutionarily conserved lysine can be targeted selectively, and the selectivity depends largely on molecular recognition of the non-covalent pharmacophore in this class of inhibitors, probably due to the moderate reactivity of the warhead. We report the first co-crystal structures of covalent inhibitor-ABL kinase domain complexes, providing insights into the interaction of this warhead with the catalytic lysine. We also employed label-free mass spectrometry to evaluate off-targets of our compounds at proteome-wide level in different mammalian cells.

Palladium-Catalzyed Atroposelective 16-Membered Macrocyclization: Total Synthesis of Isoplagiochin D?

Xi, Junwei,Gu, Zhenhua

supporting information, p. 1081 - 1085 (2020/07/06)

Isoplagiochin D is a ring-strained macrocyclic bisbibenzylis, which showed stable axial chirality in one biaryl structure, and semistable axial chirality in the other biaryl moiety. We reported here an unprecedented example for the catalytically asymmetri

Ortho-Selective C-H Borylation of Aromatic Ethers with Pinacol-borane by Organo Rare-Earth Catalysts

Xue, Can,Luo, Yong,Teng, Huailong,Ma, Yuanhong,Nishiura, Masayoshi,Hou, Zhaomin

, p. 5017 - 5022 (2018/05/14)

The regioselective C-H borylation of aromatic ethers such as anisoles is of much interest and importance, but has remained a challenge to date. We report herein the catalytic ortho-selective C-H borylation of a wide range of aromatic ethers with pinacolborane (HBpin) by rare-earth metallocene complexes. This protocol offers an efficient and straightforward route for the synthesis of a variety of borylated aromatic ether derivatives. A proper metal/ligand combination for the rare-earth metal catalysts was found to be critically important to promote this transformation.

SUBSTITUTED BICYCLIC HETEROARYL COMPOUNDS AS RXR AGONISTS

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Paragraph 0360, (2016/12/01)

The present invention relates to certain substituted bicyclic compounds that are agonists of RXR and which are therefore useful in the treatment of certain disorders that can be prevented or treated by activation of this receptor. In addition the invention relates to the compounds, methods for their preparation, pharmaceutical compositions containing the compounds and the uses of these compounds in the treatment of certain disorders.

Formal Ir-Catalyzed Ligand-Enabled Ortho and Meta Borylation of Aromatic Aldehydes via in Situ-Generated Imines

Bisht, Ranjana,Chattopadhyay, Buddhadeb

supporting information, p. 84 - 87 (2016/01/25)

The ligand-enabled development of ortho and meta C-H borylation of aromatic aldehydes is reported. It was envisaged that while ortho borylation could be achieved using tert-butylamine as the traceless protecting/directing group, meta borylation proceeds via an electrostatic interaction and a secondary interaction between the ligand of the catalyst and the substrate. These ligand-substrate electrostatic interactions and secondary B-N interactions provide an unprecedented controlling factor for meta-selective C-H activation/borylation.

SPIRO-SUBSTITUTED OXINDOLE DERIVATIVES HAVING AMPK ACTIVITY

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Page/Page column 82; 83, (2015/01/07)

The present invention relates to compounds of formula (I), which have valuable pharmacological properties, in particular are activators of AMPK and which are therefore useful in the treatment of certain disorders that can be prevented or treated by activation of this receptor. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

OLEFIN SUBSTITUTED OXINDOLES HAVING AMPK ACTIVITY

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Page/Page column 69, (2015/01/07)

The present invention relates to compounds of formula (I), which have valuable pharmacological properties, in particular are activators of AMPK and which are therefore useful in the treatment of certain disorders that can be prevented or treated by activation of this receptor. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.

Total synthesis of acerogenins E, G and K, and centrolobol

Ogura, Tetsuhiro,Usuki, Toyonobu

, p. 2807 - 2815 (2013/03/28)

The first total synthesis of the diarylheptanoid acerogenins E and K, isolated from Acer nikoense MAXIM., is described. Formation of the 13-membered m,m-cyclophane skeleton was successfully achieved on the basis of a domino process involving a Miyaura arylborylation-intramolecular Suzuki reaction. The cyclization precursor was prepared via a Wittig reaction and Claisen-Schmidt condensation, which proceeded in moderate yields. The total synthesis of acerogenin G and centrolobol was also achieved from a common synthetic intermediate.

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