U6000
Uridine 5′-monophosphomorpholidate 4-morpholine-N,N′-dicyclohexylcarboxamidine salt
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关于此项目
经验公式（希尔记法）:
C13H19N3O9P · C17H32N3O
化学文摘社编号:
分子量:
686.73
MDL编号:
UNSPSC代码:
12352204
PubChem化学物质编号:
NACRES:
NA.26
生物来源
synthetic (organic)
方案
≥97% (HPLC)
表单
powder
储存温度
−20°C
SMILES字符串
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
InChI key
RUAYLFCHPJYFJL-HVVPPSBSSA-N
应用
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).
生化/生理作用
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).
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
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