Uracil-1-yl

Base Information

Chemical Name:Uracil-1-yl
CAS No.:87009-12-9
Molecular Formula:C₇H₉N₅O₃
Molecular Weight:211.18
Hs Code.:2933599090
DSSTox Substance ID:DTXSID501007260
Nikkaji Number:J1.348.664F,J3.152.277C
Mol file:87009-12-9.mol

Synonyms:Uracil-1-yl;87009-12-9;CCRIS 3904;DTXSID501007260;(4-Hydroxypyrimidin-2-yl)oxidanyl

Suppliers and Price of Uracil-1-yl

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

American Custom Chemicals Corporation
URACIL-1-YL 95.00%
5MG
$ 497.19

Total 3 raw suppliers

Chemical Property of Uracil-1-yl

Chemical Property:

PSA：62.82000
LogP:-1.15100
XLogP3:-0.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:111.019452343
Heavy Atom Count:8
Complexity:171

Purity/Quality:: URACIL-1-YL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CN=C(NC1=O)[O]

Technology Process of Uracil-1-yl

There total 1 articles about Uracil-1-yl 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: 70.0%

: 133762-82-0
1-(3-Azido-2-hydroxy-propyl)-4-methoxy-1H-pyrimidin-2-one

: 87009-12-9
1-(3-Azido-2-hydroxypropyl)uracil

Guidance literature:: With acetic acid; at 80 ℃; for 3h;
DOI:10.1135/cccc19941153

Reference yield:

: 87009-12-9
1-(3-Azido-2-hydroxypropyl)uracil

: 123417-30-1
11-(p-tolylsulphonyloxy)-3,9-propane-8-aza-9H-xanthine

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / bromine / methanol; CH₂Cl₂ / 2 h / Ambient temperature

2: 74.1 percent / dimethylformamide / 16 h / 115 °C

3: 86.9 percent / pyridine / 5 h / Ambient temperature

With bromine; In pyridine; methanol; dichloromethane; N,N-dimethyl-formamide;