3,4-Dihydrozebularine

Base Information

Chemical Name:3,4-Dihydrozebularine
CAS No.:102922-02-1
Molecular Formula:C₉H₁₄N₂O₅
Molecular Weight:230.221
Hs Code.:
DSSTox Substance ID:DTXSID401228334
Nikkaji Number:J652.751E
Wikidata:Q27120444
Metabolomics Workbench ID:56442
ChEMBL ID:CHEMBL1232227

Synonyms:3,4-dihydrozebularine;dihydrozebularine

Suppliers and Price of 3,4-Dihydrozebularine

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

Total 0 raw suppliers

Chemical Property of 3,4-Dihydrozebularine

Chemical Property:

XLogP3:-1.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:230.09027155
Heavy Atom Count:16
Complexity:308

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C=CN(C(=O)N1)C2C(C(C(O2)CO)O)O
Isomeric SMILES:C1C=CN(C(=O)N1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)O

Technology Process of 3,4-Dihydrozebularine

There total 2 articles about 3,4-Dihydrozebularine 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: 57.0%

: 102922-01-0
C₃₀H₂₆N₂O₈

: 102922-02-1
3,4-dihydro-1-β-D-ribofuranosyl-2(1H)-pyrimidinone

Guidance literature:: With methanol; ammonia; In chloroform; at 4 ℃; for 20h;
DOI:10.1021/jm00158a009

Reference yield:

: 52523-24-7
(2R,3R,4R,5R)-2-((benzoyloxy)methyl)-5-(2-oxopyrimidin-1(2H)-yl)tetrahydrofuran-3,4-diyl dibenzoate

: 102922-02-1
3,4-dihydro-1-β-D-ribofuranosyl-2(1H)-pyrimidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / NaBH₄ / tetrahydrofuran; methanol / 1 h / 0 °C

2: 57 percent / NH₃/CH₃OH / CHCl₃ / 20 h / 4 °C

With methanol; sodium tetrahydroborate; ammonia; In tetrahydrofuran; methanol; chloroform;
DOI:10.1021/jm00158a009