U6000

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

• Formule empirique (notation de Hill): C₁₃H₁₉N₃O₉P · C₁₇H₃₂N₃O
• Numéro CAS: 24558-91-6
• Poids moléculaire : 686.73
• Numéro MDL: MFCD00078808
• Code UNSPSC : 12352204
• ID de substance PubChem : 329827640
• Nomenclature NACRES : NA.26

Propriétés

• Source biologique: synthetic (organic)
• Niveau de qualité: 200
• Pureté: ≥97% (HPLC)
• Forme: powder
• Température de stockage: −20°C
• Chaîne 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
• Clé InChI: RUAYLFCHPJYFJL-HVVPPSBSSA-N

Description

Application

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).

Actions biochimiques/physiologiques

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).

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: Eyeshields, Gloves, type N95 (US)