Skip to main content
Pseudouridine 5'-monophosphate CAS#: 1157-60-4
IdentificationPhysical DataSpectraRoute of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NamePseudouridine 5'-monophosphateIUPAC Namemethyl dihydrogen phosphateMolecular StructureCAS Registry Number 1157-60-4Synonymspseudouridine 5'-phosphatePseudouridylic acid1157-60-4Pseudouridine-5'-Monophosphate2,4(1H,3H)-Pyrimidinedione, 5-(5-O-phosphono-beta-D-ribofuranosyl)-methyl dihydrogen phosphate(1S)-1,4-anhydro-1-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-5-O-phosphono-D-ribitol{methoxy}phosphonic acidmethoxyphosphonic acidPseudouridine monophosphateSCHEMBL85139988NC65Q5EZCHEBI:18116DB03829C01168Q27102833Uracil, 5-beta-D-ribofuranosyl-, 5'-(dihydrogen phosphate)5-(5-O-Phosphono-beta-D-ribofuranosyl)-2,4(1H,3H)-pyrimidinedione5-(5-O-phosphono-beta-D-ribofuranosyl)pyrimidine-2,4(1H,3H)-dione((2R,3S,4R,5S)-5-(2,4-Dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate(1S)-1,4-anhydro-1-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-D-ribitol 5-(dihydrogen phosphate)PSUMolecular FormulaC9H13N2O9PMolecular Weight324.18InChIInChI=1S/C9H13N2O9P/c12-5-4(2-19-21(16,17)18)20-7(6(5)13)3-1-10-9(15)11-8(3)14/h1,4-7,12-13H,2H2,(H2,16,17,18)(H2,10,11,14,15)/t4-,5-,6-,7+/m1/s1InChI KeyMOBMOJGXNHLLIR-GBNDHIKLSA-NIsomeric SMILESC1=C(C(=O)NC(=O)N1)2(((O2)COP(=O)(O)O)O)O

Physical Data

AppearanceWhite solid

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)NMRNMR1H-NMR

Route of Synthesis (ROS)

Route of Synthesis (ROS) of Pseudouridine 5'-monophosphate CAS 1157-60-4

ConditionsYieldhttps://www.chemwhat.com/wp-content/uploads/2017/12/Route-of-Synthesis-ROS-of-Pseudouridine-5-monophosphate-CAS-1157-60-4.png

Safety and Hazards

No data available

Other Data

Store at -20°C for long time, in container tightly sealed; Protect from light.HS CodeStorageStore at -20°C for long time, in container tightly sealed; Protect from light.Shelf Life2 yearsMarket Price

DruglikenessLipinski rules componentMolecular Weight324.184logP-4.135HBA11HBD6Matching Lipinski Rules2Veber rules componentPolar Surface Area (PSA)184.46Rotatable Bond (RotB)4Matching Veber Rules1

Quantitative Results1 of 3Comment (Pharmacological Data)Bioactivities presentReferenceSynthesis and conformational properties of diribonucleoside monophosphates containing modified nucleosides as found in transfer RNA.2 of 3Comment (Pharmacological Data)Bioactivities present ReferenceHDHD1, which is often deleted in X-linked ichthyosis, encodes a pseudouridine-5′-phosphatase3 of 3Comment (Pharmacological Data)Bioactivities present ReferenceHDHD1, which is often deleted in X-linked ichthyosis, encodes a pseudouridine-5′-phosphatase

Use PatternPseudouridine 5'-monophosphate CAS#: 1157-60-4 purity 96% min and is used be a IVD
https://www.chemwhat.com/pseudouridine-5-monophosphate-cas-1157-60-4/

Comments

Popular posts from this blog

BCB (Benzocyclobutene): — Watson International Enables the Transition from Concept to Scalable Application

Benzocyclobutene (BCB) is an organic compound with a rigid molecular structure composed of a conjugated benzene ring and a four-membered ring. Its excellent thermal stability and electrical properties have made it a highly promising candidate for next-generation electronic materials. Historically, its industrial adoption has been constrained by high production costs, complex purification processes, and limited output. However, with growing demand in high-end applications and recent advances in upstream technology, BCB is now poised for industrial-scale deployment. Material Properties and Structural Advantages BCB (C₈H₈) is a non-polar molecule, free of ester, carboxyl, or amide groups, giving it excellent dielectric properties and low moisture absorption. Its dielectric constant (Dk) and dissipation factor (Df) remain stable across wide temperature and frequency ranges—key metrics for ensuring signal integrity in high-frequency, high-speed communication systems. Unlike conventional m...

BCB (Benzocyclobutene): — Watson International Enables the Transition from Concept to Scalable Application

Despite BCB’s well-established performance advantages, its commercialization has long been hindered by production cost and scalability challenges. Watson International has made critical breakthroughs in BCB industrialization through integrated innovation in synthesis, purification, and material formulation: Cost Reduction: By optimizing synthetic pathways and improving by-product recovery, Watson has significantly reduced the unit production cost of BCB, enabling cost-effective scaling; High Purity Production: Advanced purification and process control technologies ensure high-purity BCB under mass-production conditions—meeting stringent requirements from high-end electronic manufacturers; Versatile Co-polymerization: Watson’s BCB materials are compatible with other advanced resins such as BMI and PPO, allowing for custom co-polymer design and performance tuning.

The World's Largest Producer of Squaric Acid Emerges: Watson Leads the Way

In a groundbreaking development for the chemical industry, Watson has officially claimed the title of the world’s largest producer of squaric acid. This achievement marks a significant milestone, positioning the company as a global leader in the production of this highly versatile compound, widely valued in pharmaceuticals, polymer research, and advanced materials. What is Squaric Acid? Squaric acid, also known as quadratic acid, is a four-carbon cyclic diketone with two ketone groups and two hydroxyl groups arranged symmetrically. It is renowned for its stability and strong acidity, making it a unique compound in both organic and inorganic chemistry. Its derivatives find applications in creating advanced coatings, conductive polymers, and as intermediates in drug synthesis. Watson: Redefining Excellence in Squaric Acid Production Watson’s rise to the top of the squaric acid industry is backed by its unmatched production capacity, cutting-edge technology, and unwavering commitment...