O-beta-D-glucosyl-trans-zeatin

Base Information

• Chemical Name: O-beta-D-glucosyl-trans-zeatin
• CAS No.: 56329-06-7
• Molecular Formula: C16H23N5O6
• Molecular Weight: 381.389
• DSSTox Substance ID: DTXSID301346498
• Nikkaji Number: J510.863B
• Wikidata: Q27104440
• Metabolomics Workbench ID: 52217
• Mol file: 56329-06-7.mol

Synonyms:O-beta-D-glucosyl-trans-zeatin;trans-Zeatin-O-glucoside;56329-06-7;O-beta-D-Glucosylzeatin;(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-2-methyl-4-(7H-purin-6-ylamino)but-2-enoxy]oxane-3,4,5-triol;Zeatine O-glucoside;CHEBI:38266;DTXSID301346498;C03423;Q27104440;6-(4-O-beta-D-Glucosyl-3-methyl-trans-but-2-enyl-amino)-purine;(2E)-2-methyl-4-(9H-purin-6-ylamino)but-2-en-1-yl beta-D-glucopyranoside

Chemical Property of O-beta-D-glucosyl-trans-zeatin

Chemical Property:

• PSA: 165.87000
• LogP: -1.39940
• Storage Temp.: −20°C
• XLogP3: -0.9
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 7
• Exact Mass: 381.16483347
• Heavy Atom Count: 27
• Complexity: 512

Purity/Quality:

99.3% ^*data from raw suppliers

trans-Zeatin-9-glucoside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=CCNC1=NC=NC2=C1NC=N2)COC3C(C(C(C(O3)CO)O)O)O
• Isomeric SMILES: C/C(=C\CNC1=NC=NC2=C1NC=N2)/CO[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O
• Uses: trans-Zeatin-O-glucoside (cZOG) plays a role in regulating the plant growth regulators in an effort to understand their growth and hormonal physiology.

Technology Process of O-beta-D-glucosyl-trans-zeatin

There total 1 articles about O-beta-D-glucosyl-trans-zeatin 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:

→ trans-zeatin O-β-D-glucopyranoside (56329-06-7)

Guidance literature:

Reference yield:

trans-zeatin O-β-D-glucopyranoside (56329-06-7) → N6-(2-isopentenyl)adenine (2365-40-4)

Guidance literature:

With β-glucosidase; at 37 ℃; for 3h;

DOI:10.1016/0031-9422(81)85156-4

Reference yield:

trans-zeatin O-β-D-glucopyranoside (56329-06-7) + benzoic acid anhydride (93-97-0) → C44H39N5O10

Guidance literature:

With 1-methyl-1H-imidazole; In acetonitrile; at 37 ℃; for 0.5h;

DOI:10.1021/ac0499017

Downstream raw materials:

N₆-(2-isopentenyl)adenine