Category: 14963-96-3

Related Products of 14963-96-3, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 14963-96-3, Name is 4-Methoxyisobenzofuran-1,3-dione,introducing its new discovery.

The compounds are substituted hydrazinophthalazines which are active as beta-adrenergic blocking agents and as vasodilators. A specific compound of the invention is 5-(3-t-butylamino-2-hydroxypropoxy)-1-hydrazinophthalazine.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2858O – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. Safety of 4-Methoxyisobenzofuran-1,3-dione, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 14963-96-3

A variety of enol lactones can be prepared through simple and inexpensive solid/liquid phase Wittig condensations of cyclic anhydrides with phosphonium salts.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2886O – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. Application In Synthesis of 4-Methoxyisobenzofuran-1,3-dione, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 14963-96-3

The present invention relates to a novel benzenedicarboxamide derivative and the use thereof as an insecticide having the formula (I) wherein the chemical groups W1 to W9, and R1 to R3 are as defined here-in.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2860O – PubChem

14963-96-3, Name is 4-Methoxyisobenzofuran-1,3-dione, belongs to benzofurans compound, is a common compound. Formula: C9H6O4In an article, once mentioned the new application about 14963-96-3.

9-amino-9-deoxydaunomycin and related compounds, in which the hydroxyl group at the 9-position of daunomycin is replaced by an amino group, have been synthesized.Asymmetry was introduced into the synthetic sequence for the AB synthon by resolution of the intermediate amino ester or acetamido acid to afford (R)-(-)-2-acetyl-2-acetamido-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene, which was converted to the tetracyclic amido ketones by Friedel-Crafts acylation with phthalic anhydride or its 3-methoxy derivative.The resulting regioisomers 4- and 1-methoxy compounds were separed, after methylation and selective demethylation, by crystallization and preparative TLC.The required introduction of the C7-hydroxyl function proceeded stereosepcifically via a three-step reaction sequence involving formation of an oxazine compound.The silver trifluoromethane assisted glycosidation of the resulting aglycons with 2-deoxy-3,4-di-O-acetyl-D-erythro-pentopyranosyl bromide or N,O-bis(trifluoroacetyl)daunosaminyl chloride, followed by alkaline hydrolysis afforded the target glycosides.The work reported herein comprises an efficient, practical synthesis of 9-amino-9-deoxydaunomycin and its analogues with the same stereochemistry as in the naturally occurring anthracyclines.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2873O – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. name: 4-Methoxyisobenzofuran-1,3-dione, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 14963-96-3

A series of novel types of 7-(4,6-dimethoxypyrimidin-2-yl)oxy – and -thio-3-methyl-1 (3H)-isobenzofuranones were discovered at Dr R Maag AG. From the thio-isobenzofuranyl series, CGA 279 233 – BSI-proposed common name pyriftalid – was chosen for further development as a grass herbicide for use in rice. General synthetic approaches to these new phthalic acid-derived compounds are given, with emphasis on the synthesis of pyriftalid and its physico-chemical behaviour.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2876O – PubChem

Electric Literature of 14963-96-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.14963-96-3, Name is 4-Methoxyisobenzofuran-1,3-dione, molecular formula is C9H6O4. In a article，once mentioned of 14963-96-3

A series of analogs of the immunomodulary drugs lenalidomide (1) and pomalidomide (2), in which the amino group is replaced with various isosteres, was prepared and assayed for immunomodulatory activity and activity against cancer cell lines. The 4-methyl and 4-chloro analogs 4 and 15, respectively, displayed potent inhibition of tumor necrosis factor-alpha (TNF-alpha) in LPS-stimulated hPBMC, potent stimulation of IL-2 in a human T cell co-stimulation assay, and anti-proliferative activity against the Namalwa lymphoma cell line. Both of these analogs displayed oral bioavailability in rat.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2881O – PubChem

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. category: benzofuran, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 14963-96-3, name is 4-Methoxyisobenzofuran-1,3-dione. In an article，Which mentioned a new discovery about 14963-96-3

The invention provides combinations comprising (or consisting essentially of) one or more ancillary compound(s) and a compound of the formula (I): or salts, tautomers, solvates and N-oxides thereof; wherein R1 is hydroxy or hydrogen; R2 is hydroxy; methoxy or hydrogen; provided that at least one of R1 and R2 is hydroxy; R3 is selected from hydrogen; halogen; cyano; optionally substituted C1-5 hydrocarbyl and optionally substituted C1-5 hydrocarbyloxy; R4 is selected from hydrogen; a group -(O) n -R7 where n is 0 or 1 and R7 is an optionally substituted acyclic C1-5 hydrocarbyl group or a monocyclic carbocyclic or heterocyclic group having 3 to 7 ring members; halogen; cyano; hydroxy; amino; and optionally substituted mono- or di-C1-5 hydrocarbyl-amino; or R3 and R4 together form a monocyclic carbocyclic or heterocyclic ring of 5 to 7 ring members; and NR5 R6 forms an optionally substituted bicyclic heterocyclic group having 8 to 12 ring members of which up to 5 ring members are heteroatoms selected from oxygen, nitrogen and sulphur. The combinations have activity as Hsp90 and/or glycogen synthase kinase-3 and/or cyclin dependent kinase and/or aurora kinase inhibitors

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2847O – PubChem

Reference of 14963-96-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.14963-96-3, Name is 4-Methoxyisobenzofuran-1,3-dione, molecular formula is C9H6O4. In a Patent，once mentioned of 14963-96-3

There are provided o-carboxy-(5-oxo-2-imidazolin-2-yl)benzo-(5-membered)-heterocyclic compounds and derivatives thereof and a method for the use therewith to control monocotyledenous and dicotyledenous plant species.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2849O – PubChem

Application of 14963-96-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.14963-96-3, Name is 4-Methoxyisobenzofuran-1,3-dione, molecular formula is C9H6O4. In a Article，once mentioned of 14963-96-3

Synthesis of daunomycinone (2) and gamma-rhodomycinone (3) by regioselective addition of the Grignard reagents 9b and 9d to the anhydride 4.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2864O – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. name: 4-Methoxyisobenzofuran-1,3-dione, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 14963-96-3

Microwave assisted cyclization of several 2-thenoylbenzoic acids 2 catalysed with clays in dry media is studied.Some clays were tested and Montmorillonite K-10, free of quarz and feldspar, was shown to be an effective catalyst for their easy conversion into the corresponding heterocyclic fused quinone in good yields.A specific effect of microwave irradiation accelerating the reaction with respect to conventional heating in the same conditions is observed.

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Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2861O – PubChem