Nom du produit:(5-(3,5-dimethylisoxazol-4-yl)thiophen-2-yl)boronic acid
IUPAC Name:[5-(3,5-dimethyl-1,2-oxazol-4-yl)thiophen-2-yl]boronic acid
- CAS：1121529-19-8
- Formule moléculaire：C9H10BNO3S
- Pureté：95%
- Numéro de catalogue：CM136283
- Poids moléculaire：223.05
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1121529-19-8
- Formule moléculaire:C9H10BNO3S
- Point de fusion:-
- Code SMILES:CC1=C(C2=CC=C(B(O)O)S2)C(C)=NO1
- Densité:
- Numéro de catalogue:CM136283
- Poids moléculaire:223.05
- Point d'ébullition:
- N° Mdl:MFCD16877474
- 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.
- Boronic Acids and Esters
- Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
- Boronic Acid For Sale
- Find trusted boronic acid for sale. Any requirements and problems can ask us at any time.
- Isoxazoles
- Isoxazole is a liquid heterocyclic compound C3H3NO isomeric with oxazole and having a penetrating odor like that of pyridine. Isoxazoles belong to an important class of five-membered aromatic heterocycles containing two electronegative heteroatoms, nitrogen and oxygen, in a 1,2-relationship and three regular sp2 carbon atoms. These molecules are found to be key components in various synthetic products in daily use and also present as a pharmacophore essential for biological activity in many drugs and bioactive natural products. In addition, isoxazoles have demonstrated their ability to exhibit hydrogen bond donor/acceptor interactions with a variety of enzymes and receptors.
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