cas 1039922-41-2|| where to buy 3-{[(4-hydroxypyrimidin-2-yl)sulfanyl]methyl}-1-benzofuran-2-carboxylic acid

Nom du produit:3-{[(4-hydroxypyrimidin-2-yl)sulfanyl]methyl}-1-benzofuran-2-carboxylic acid

IUPAC Name:3-{[(4-hydroxypyrimidin-2-yl)sulfanyl]methyl}-1-benzofuran-2-carboxylic acid

: CAS：1039922-41-2; Formule moléculaire：C14H10N2O4S; Pureté：95%+

Unité d'emballage	Stock disponible	Prix($)
CM475215-250mg	3-4 Weeks	ȃƓƥ
CM475215-500mg	3-4 Weeks	ƥǵƥ
CM475215-1g	3-4 Weeks	ŹĲŗ

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: N° CAS:1039922-41-2; Formule moléculaire:C14H10N2O4S; Point de fusion:-; Code SMILES:OC(=O)C1=C(CSC2=NC(O)=CC=N2)C2=CC=CC=C2O1; Densité:

: Numéro de catalogue:CM475215; Poids moléculaire:302.3; Point d'ébullition:; N° Mdl:MFCD13383585; Stockage:

: Pyrimidines; Pyrimidine, also known as 1,3-diazobenzene, is a heterocyclic compound with the chemical formula C4H4N2. Pyrimidine is formed by substituting 2 nitrogen atoms for 2 carbons in the meta-position of benzene. It is a diazine and retains its aromaticity. Derivatives of pyrimidine widely exist in organic macromolecular nucleic acids, and many drugs also contain pyrimidine rings. In nucleic acids, three nucleobases are pyrimidine derivatives: cytosine, thymine and uracil. There are a variety of pyrimidine-containing drugs on the market, most of which are kinase inhibitors.

: Benzofurans; Benzofuran is an aromatic heterocyclic organic compound with the chemical formula C8H6O. It is a colorless oily liquid at room temperature with an aromatic odor. Benzofuran can be volatilized with water vapor and can be decomposed by potassium permanganate and other oxidants. It is an intermediate for the preparation of amiodarone and indene resin. Benzofuran derivatives are important pharmaceutical intermediates.; Benzofuran | C8H6O | CID 9223 -Chemenu; Benzofuran | C8H6O | CID 9223 |Where to Buy Benzofurans; Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings. This colourless liquid is a component of coal tar.Benzofuran is extracted from coal tar. It is also obtained by dehydrogenation of 2-ethylphenol.