Name: Uridine 5′-monophosphomorpholidate 4-morpholine-N,N′-dicyclohexylcarboxamidine salt
Brand: SIGMA

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About This Item

Empirical Formula (Hill Notation):

C₁₃H₁₉N₃O₉P · C₁₇H₃₂N₃O

CAS Number:

24558-91-6

Molecular Weight:

686.73

MDL number:

MFCD00078808

UNSPSC Code:

12352204

PubChem Substance ID:

329827640

NACRES:

NA.26

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biological source

synthetic (organic)

Quality Level

200

Assay

≥97% (HPLC)

form

powder

storage temp.

−20°C

SMILES string

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

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).

Biochem/physiol Actions

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).

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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