1-(2-amino-4-oxopteridin-7-yl)-1-oxo-2,3,4-butanetriol-2,4-cyclic phosphate

Base Information

• Chemical Name: 1-(2-amino-4-oxopteridin-7-yl)-1-oxo-2,3,4-butanetriol-2,4-cyclic phosphate
• CAS No.: 122856-31-9
• Molecular Formula: C₁₀H₁₀N₅O₇P
• Molecular Weight: 343.192
• Mol file: 122856-31-9.mol

Synonyms:4(1H)-Pteridinone,2-amino-6-[(2,5-dihydroxy-1,3,2-dioxaphosphorinan-4-yl)carbonyl]-, P-oxide;4(1H)-Pteridinone,2-amino-6-[[(4S,5R)-2,5-dihydroxy-2-oxido-1,3,2-dioxaphosphorinan-4-yl]carbonyl]-(9CI); 1,3,2-Dioxaphosphorinane, 4(1H)-pteridinone deriv.; Compound Z

Chemical Property of 1-(2-amino-4-oxopteridin-7-yl)-1-oxo-2,3,4-butanetriol-2,4-cyclic phosphate

Chemical Property:

• Vapor Pressure: 3.37E-22mmHg at 25°C
• Boiling Point: 727.2°C at 760 mmHg
• Flash Point: 393.6°C
• PSA: 201.41000
• Density: 2.39g/cm³
• LogP: -1.30290

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 1-(2-amino-4-oxopteridin-7-yl)-1-oxo-2,3,4-butanetriol-2,4-cyclic phosphate

There total 2 articles about 1-(2-amino-4-oxopteridin-7-yl)-1-oxo-2,3,4-butanetriol-2,4-cyclic phosphate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C10H12N5O7P → C10H10N5O7P (122856-31-9)

Guidance literature:

With iodine; potassium iodide; at 20 ℃; for 0.333333h; pH=2;

DOI:10.1021/ja401781t

Reference yield:

(8S)-3′,8-cyclo-7,8-dihydroguanosine 5′-triphosphate → C10H10N5O7P (122856-31-9)

Guidance literature:

Multi-step reaction with 2 steps

1: MoaC from S_. aureus; ammonium bicarbonate / 0.33 h / 25 °C / pH 9.1 / Inert atmosphere; Enzymatic reaction

2: potassium iodide; iodine / 0.33 h / 20 °C / pH 2

With MoaC from S_. aureus; iodine; ammonium bicarbonate; potassium iodide;

DOI:10.1021/ja401781t

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