cis-Zeatin riboside

Base Information

Chemical Name:cis-Zeatin riboside
CAS No.:15896-46-5
Molecular Formula:C15H21N5O5
Molecular Weight:351.35800
Hs Code.:
DSSTox Substance ID:DTXSID801017777
Metabolomics Workbench ID:163713
Nikkaji Number:J486.816A
Wikidata:Q27103082
Mol file:15896-46-5.mol

Synonyms:N-(4-hydroxy-3-methyl-2-butenyl)adenosine;ribosylzeatin;zeatin riboside;zeatin riboside, (cis-(Z))-isomer;zeatin riboside, (E)-isomer

Suppliers and Price of cis-Zeatin riboside

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
cis-Zeatin riboside
10 mg
$ 950.00

Biosynth Carbosynth
cis-Zeatin riboside
5 mg
$ 620.00

Biosynth Carbosynth
cis-Zeatin riboside
2 mg
$ 340.00

Biosynth Carbosynth
cis-Zeatin riboside
1 mg
$ 190.00

Biosynth Carbosynth
cis-Zeatin riboside
25 mg
$ 1750.00

AK Scientific
cis-Zeatinriboside
5mg
$ 1670.00

Total 7 raw suppliers

Chemical Property of cis-Zeatin riboside

Chemical Property:

Boiling Point:731.8±70.0 °C(Predicted)
PKA:13.11±0.70(Predicted)
PSA：145.78000
Density:1.65±0.1 g/cm3(Predicted)
LogP:-1.13870
XLogP3:-0.1
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:6
Exact Mass:351.15426879
Heavy Atom Count:25
Complexity:481

Purity/Quality:

98%, ^*data from raw suppliers

cis-Zeatin riboside ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCNC1=C2C(=NC=N1)N(C=N2)C3C(C(C(O3)CO)O)O)CO
Isomeric SMILES:C/C(=C/CNC1=C2C(=NC=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)/CO
Uses cis-Zeatin Riboside acts as phosphate starvation response hormone that stimulates root and root hair elongation to enlarge root absorbing surface and to increased phosphate concentration in roots.

Technology Process of cis-Zeatin riboside

There total 3 articles about cis-Zeatin riboside 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: 44.0%

: 7724-76-7,33156-15-9
6-N-(3,3-dimethylallyl)adenosine

: 6025-53-2,15896-46-5,28542-78-1,91928-28-8,91928-29-9
6-((E)-4-hydroxy-3-methylbut-2-enylamino)-9-β-D-ribofuranosylpurine

Guidance literature:: With tert.-butylhydroperoxide; selenium(IV) oxide; In dichloromethane; benzene; at 32 ℃;
DOI:10.1016/S0040-4039(00)86749-0

Reference yield: 38.0%

: 6025-53-2,15896-46-5,28542-78-1,91928-28-8,91928-29-9
6-((E)-4-hydroxy-3-methylbut-2-enylamino)-9-β-D-ribofuranosylpurine

: 6025-53-2,15896-46-5,28542-78-1,91928-28-8,91928-29-9
6-((Z)-4-hydroxy-3-methylbut-2-enylamino)-9-β-D-ribofuranosylpurine

Guidance literature:: In ethanol; for 48h; Irradiation;
DOI:10.1016/S0040-4039(00)86749-0

Reference yield:

: 7724-76-7,33156-15-9
6-N-(3,3-dimethylallyl)adenosine

: 6025-53-2,15896-46-5,28542-78-1,91928-28-8,91928-29-9
6-((Z)-4-hydroxy-3-methylbut-2-enylamino)-9-β-D-ribofuranosylpurine

Guidance literature:: Multi-step reaction with 2 steps

1: 44 percent / SeO₂, ter-butyl hydroperoxide / benzene; CH₂Cl₂ / 32 °C

2: 38 percent / ethanol / 48 h / Irradiation

With tert.-butylhydroperoxide; selenium(IV) oxide; In ethanol; dichloromethane; benzene;
DOI:10.1016/S0040-4039(00)86749-0