Nom du produit:5-bromo-N-[4-(7-methoxy-1-benzofuran-2-yl)-1,3-thiazol-2-yl]thiophene-2-carboxamide
IUPAC Name:5-bromo-N-[4-(7-methoxy-1-benzofuran-2-yl)-1,3-thiazol-2-yl]thiophene-2-carboxamide
- CAS:921550-71-2
- Formule moléculaire:C17H11BrN2O3S2
- Pureté:95%+
- Numéro de catalogue:CM901111
- Poids moléculaire:435.31
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Détails du produit
- N° CAS:921550-71-2
- Formule moléculaire:C17H11BrN2O3S2
- Point de fusion:-
- Code SMILES:COC1=C2OC(=CC2=CC=C1)C1=CSC(NC(=O)C2=CC=C(Br)S2)=N1
- Densité:
- Numéro de catalogue:CM901111
- Poids moléculaire:435.31
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Thiophenes
- Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
- Thiazoles
- Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.
- 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.