![N-[4-(5-chloro-1,3-benzoxazol-2-yl)phenyl]thiophene-2-carboxamide](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F104163-n-4-5-chloro-13-benzoxazol-2-yl-phenyl-thiophene-2-carboxamide.webp&w=3840&q=75)
CAS 5750-74-3: N-[4-(5-chloro-1,3-benzoxazol-2-yl)phenyl]thiophene-2-carboxamide
Formula:C18H11ClN2O2S
InChI:InChI=1/C18H11ClN2O2S/c19-12-5-8-15-14(10-12)21-18(23-15)11-3-6-13(7-4-11)20-17(22)16-2-1-9-24-16/h1-10H,(H,20,22)
SMILES:c1cc(C(=Nc2ccc(cc2)c2nc3cc(ccc3o2)Cl)O)sc1
Synonyms:- 2-thiophenecarboxamide, N-[4-(5-chloro-2-benzoxazolyl)phenyl]-
- 2,5-dichloro-4-methoxypyrimidine
Sort by
Found 5 products.
2,5-Dichloro-4-methoxypyrimidine
CAS:2,5-Dichloro-4-methoxypyrimidine (2,5-DCP) is a heterocyclic compound that has been synthesized using a microwave irradiation technique. The microwave irradiation facilitates the generation of 2,5-DCP in high yields and in shorter times than conventional heating methods. This compound was synthesized by reacting phenylboronic acid with 4,5-dichloropyrimidine in the presence of palladium as catalyst and boron trifluoride etherate as additive. The regioselectivity of this reaction can be controlled by varying the ratio of phenylboronic acid to 4,5-dichloropyrimidine. 2,5-DCP can also be obtained by cross-coupling reactions between phenylboronic acids and arylpyrimidines. This synthetic strategy is efficient and provides regioselective products.Formula:C5H4Cl2N2OPurity:Min. 95%Molecular weight:179 g/molRef: 3D-FD175209
Discontinued product2,5-dichloro-4-methoxypyrimidine
CAS:Formula:C5H4Cl2N2OPurity:97%Color and Shape:SolidMolecular weight:179.00412,5-Dichloro-4-methoxypyrimidine
CAS:2,5-Dichloro-4-methoxypyrimidinePurity:97%Molecular weight:179.00g/mol
