Xylocytidine

Base Information

Chemical Name:Xylocytidine
CAS No.:3530-56-1
Molecular Formula:C9H13 N3 O5
Molecular Weight:243.219
Hs Code.:
DSSTox Substance ID:DTXSID60188813
Nikkaji Number:J608.994A
Wikidata:Q83060662
ChEMBL ID:CHEMBL2448171
Mol file:3530-56-1.mol

Synonyms:beta-xylocytidine;xyloC;xylocytidine

Suppliers and Price of Xylocytidine

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

Biosynth Carbosynth
1-(b-D-Xylofuranosyl)cytosine
50 mg
$ 325.00

Biosynth Carbosynth
1-(b-D-Xylofuranosyl)cytosine
25 mg
$ 200.00

Biosynth Carbosynth
1-(b-D-Xylofuranosyl)cytosine
10 mg
$ 125.00

Biosynth Carbosynth
1-(b-D-Xylofuranosyl)cytosine
5 mg
$ 75.00

Biosynth Carbosynth
1-(b-D-Xylofuranosyl)cytosine
100 mg
$ 500.00

AK Scientific
1-(beta-D-Xylofuranosyl)cytosine
50mg
$ 488.00

Total 14 raw suppliers

Chemical Property of Xylocytidine

Chemical Property:

PSA：131.82000
LogP:-2.22060
XLogP3:-2.1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:243.08552052
Heavy Atom Count:17
Complexity:383

Purity/Quality:

99%, ^*data from raw suppliers

1-(b-D-Xylofuranosyl)cytosine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)O
Isomeric SMILES:C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@H]([C@H](O2)CO)O)O

Technology Process of Xylocytidine

There total 9 articles about Xylocytidine 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: 87.0%

: 160946-66-7
1-(2,3,5-tri-O-acetyl-β-L-arabinofuranosyl)-4-(1,2,4-triazole-1-yl)-1H-pyridinium-2-one

: 65-46-3,147-94-4,3083-52-1,3530-56-1,6880-73-5,7428-39-9,13913-16-1,16033-23-1,16110-07-9,18265-49-1,20566-05-6,21967-64-6,26524-60-7,27921-78-4,36684-85-2,77172-20-4,89618-11-1
1-β-L-arabinofuranosyl cytosine

Guidance literature:: With ammonium hydroxide; In 1,4-dioxane; for 48h; Ambient temperature;
DOI:10.1080/15257779408010669

Reference yield: 86.0%

: 1382804-49-0
2',3',5'-tri-O-benzoyl-ara-L-cytidine

: 65-46-3,147-94-4,3083-52-1,3530-56-1,6880-73-5,7428-39-9,13913-16-1,16033-23-1,16110-07-9,18265-49-1,20566-05-6,21967-64-6,26524-60-7,27921-78-4,36684-85-2,77172-20-4,89618-11-1
1-β-L-arabinofuranosyl cytosine

Guidance literature:: With methanol; sodium methylate; at 20 ℃; for 4h;
DOI:10.1080/15257770.2012.689410

Reference yield:

: ancitabine

: 65-46-3,147-94-4,3083-52-1,3530-56-1,6880-73-5,7428-39-9,13913-16-1,16033-23-1,16110-07-9,18265-49-1,20566-05-6,21967-64-6,26524-60-7,27921-78-4,36684-85-2,77172-20-4,89618-11-1
1-β-L-arabinofuranosyl cytosine

: 58-96-8,3083-77-0,3258-07-9,3565-16-0,4348-60-1,4348-61-2,4348-71-4,4401-72-3,4433-38-9,16535-78-7,20289-55-8,20289-61-6,24259-58-3,26287-69-4,26524-61-8,36684-86-3,40093-89-8,41545-81-7,41545-82-8
1-(β-L-arabinofuranosyl)-uracil

Guidance literature:: With sodium dihydrogenphosphate; In water; at 60 ℃; Kinetics; Rate constant; Mechanism; hydrolysis under different reaction conditions;
DOI:10.1002/jps.2600730709