U6000

Uridine 5′-monophosphomorpholidate 4-morpholine-N,N′-dicyclohexylcarboxamidine salt

• Fórmula empírica (Notação de Hill): C₁₃H₁₉N₃O₉P · C₁₇H₃₂N₃O
• Número CAS: 24558-91-6
• Peso molecular: 686.73
• Número MDL: MFCD00078808
• Código UNSPSC: 12352204
• ID de substância PubChem: 329827640
• NACRES: NA.26

Propriedades

• fonte biológica: synthetic (organic)
• Ensaio: ≥97% (HPLC)
• forma: powder
• temperatura de armazenamento: −20°C
• cadeia de caracteres SMILES: C1CCC(CC1)N\C(=N\C2CCCCC2)N3CCOCC3.O[C@H]4[C@@H](O)[C@@H](O[C@@H]4COP(O)(=O)N5CCOCC5)N6C=CC(=O)NC6=O
• InChI: 1S/C17H31N3O.C13H20N3O9P/c1-3-7-15(8-4-1)18-17(20-11-13-21-14-12-20)19-16-9-5-2-6-10-16;17-9-1-2-16(13(20)14-9)12-11(19)10(18)8(25-12)7-24-26(21,22)15-3-5-23-6-4-15/h15-16H,1-14H2,(H,18,19);1-2,8,10-12,18-19H,3-7H2,(H,21,22)(H,14,17,20)/t;8-,10-,11-,12-/m.1/s1
• chave InChI: RUAYLFCHPJYFJL-HVVPPSBSSA-N

Descrição

Aplicação

Uridine 5′-monophosphomorpholidate 4-morpholine-N,N′-dicyclohexylcarboxamidine salt has been used in the synthesis of UDP-TEMPO (uridine 5′-diphospho-4-O-2,2,6,6-tetramethylpiperidine 1-oxyl).

Ações bioquímicas/fisiológicas

Uridine5′-monophosphomorpholidate 4-morpholine-N,N′-dicyclohexylcarboxamidine salt, also known as UMP-morpholidate, is used as a reactant in the synthesis of uridine5′-(2,3,4-tri-O-acetyl-6-S-acetyl-6-thio-α-d-galactopyranosyldiphosphate). UMP-morpholidate serves as a key reactant in the Khorana-Moffatt procedure for synthesizing uridine diphosphate (UDP)-sugar nucleotides.Uridine 5′-monophosphomorpholidate 4-morpholine-N,N′-dicyclohexylcarboxamidine salt can be used for the synthesis of UDP-azido-GalNAc (uridine diphosphate N-azido acetylgalactosamine).

Informações de segurança

• Código de classe de armazenamento: 11 - Combustible Solids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable
• Equipamento de proteção individual: Eyeshields, Gloves, type N95 (US)