5-(3-Methoxy-3-oxoprop-1-en-1-yl)uridine

Base Information

Chemical Name:5-(3-Methoxy-3-oxoprop-1-en-1-yl)uridine
CAS No.:58931-19-4
Molecular Formula:C13H16N2O8
Molecular Weight:328.27
Hs Code.:
DSSTox Substance ID:DTXSID40705623
Mol file:58931-19-4.mol

Synonyms:58931-19-4;SCHEMBL6888282;DTXSID40705623;5-(3-Methoxy-3-oxoprop-1-en-1-yl)uridine

Suppliers and Price of 5-(3-Methoxy-3-oxoprop-1-en-1-yl)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

TRC
(E)-5-(2-Carbomethoxyvinyl)uridine
50mg
$ 95.00

American Custom Chemicals Corporation
(E)-5-(2-CARBOMETHOXYVINYL)URIDINE 95.00%
5MG
$ 500.53

Total 5 raw suppliers

Chemical Property of 5-(3-Methoxy-3-oxoprop-1-en-1-yl)uridine

Chemical Property:

PSA：151.08000
LogP:-2.66570
XLogP3:-1.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:5
Exact Mass:328.09066547
Heavy Atom Count:23
Complexity:572

Purity/Quality:

≥ 97% ^*data from raw suppliers

(E)-5-(2-Carbomethoxyvinyl)uridine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)C=CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O
Isomeric SMILES:COC(=O)C=CC1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O
Uses (E)-5-(2-Carbomethoxyvinyl)uridine can be used as a reactant/reagent in preparation of modified nucleosides, nucleotides, and nucleic acids, and uses thereof for human granulocyte-colony stimulating factor-modified mRNA-induced cell proliferation.

Technology Process of 5-(3-Methoxy-3-oxoprop-1-en-1-yl)uridine

There total 5 articles about 5-(3-Methoxy-3-oxoprop-1-en-1-yl)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: 86.0%