3-(3-Amino-3-carboxypropyl)uridine

Base Information

Chemical Name:3-(3-Amino-3-carboxypropyl)uridine
CAS No.:52745-94-5
Molecular Formula:C₁₃H₁₉N₃O₈
Molecular Weight:345.309
Hs Code.:
DSSTox Substance ID:DTXSID10967195
Nikkaji Number:J2.140.791G
Wikidata:Q27109263
Metabolomics Workbench ID:53728
Mol file:52745-94-5.mol

Synonyms:3-(3-amino-3-carboxypropyl)uridine;nucleoside X

Suppliers and Price of 3-(3-Amino-3-carboxypropyl)uridine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

AK Scientific
3-(3-Amino-3-carboxypropyl)uridine
500mg
$ 2412.00

AK Scientific
3-(3-Amino-3-carboxypropyl)uridine
250mg
$ 1400.00

Total 5 raw suppliers

Chemical Property of 3-(3-Amino-3-carboxypropyl)uridine

Chemical Property:

Vapor Pressure:1.08E-20mmHg at 25°C
Boiling Point:667.9°Cat760mmHg
PKA:2.20±0.10(Predicted)
Flash Point:357.8°C
PSA：177.24000
Density:1.643g/cm³
LogP:-2.87620
XLogP3:-5
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:6
Exact Mass:345.11721457
Heavy Atom Count:24
Complexity:553

Purity/Quality:

97% ^*data from raw suppliers

3-(3-Amino-3-carboxypropyl)uridine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CN(C(=O)N(C1=O)CCC(C(=O)O)N)C2C(C(C(O2)CO)O)O
Isomeric SMILES:C1=CN(C(=O)N(C1=O)CCC(C(=O)O)N)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O
Uses 3-(3-Amino-3-carboxypropyl)uridine is a naturally occurring nucleotide and a metabolite of Uridine. Uridine is a nucleoside widely distributed in nature. Uridine is one of the four basic components of ribonucleic acid (RNA).

Technology Process of 3-(3-Amino-3-carboxypropyl)uridine

There total 5 articles about 3-(3-Amino-3-carboxypropyl)uridine 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:

: 2-Acetylamino-4-[3-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-butyric acid

: 52745-94-5
3-(3-amino-3-carboxypropyl)uridine

Guidance literature:: With Acylase I; In water; at 38 ℃; pH=7.3;

Reference yield:

: 77181-75-0
2-Acetylamino-4-[3-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-butyramide

: 52745-94-5
3-(3-amino-3-carboxypropyl)uridine

Guidance literature:: With hydrogenchloride; at 80 ℃; for 2h;

Reference yield:

: 77181-77-2
2-Acetylamino-4-[3-((2R,3R,4S,5R)-3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-butyric acid methyl ester

: 52745-94-5
3-(3-amino-3-carboxypropyl)uridine

Guidance literature:: Multi-step reaction with 2 steps

1: aq. LiOH / 6 h / Ambient temperature

2: acylase I / H₂O / 38 °C / pH=7.3

With lithium hydroxide; Acylase I; In water;