Gibberellin A53

Base Information

Chemical Name:Gibberellin A53
CAS No.:51576-08-0
Molecular Formula:C20H28O5
Molecular Weight:348.4333
Hs Code.:
DSSTox Substance ID:DTXSID20331540
Nikkaji Number:J4.770H
Wikidata:Q27103126
Metabolomics Workbench ID:28564
Mol file:51576-08-0.mol

Synonyms:Gibberellin A53;51576-08-0;GA53;(1S,2S,3S,4R,8S,9S,12S)-12-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid;gibberellin 53;CHEBI:27433;DTXSID20331540;LMPR0104170007;(1S,2S,3S,4R,8S,9S,12S)-12-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0(1,9).0(3,8)]pentadecane-2,4-dicarboxylic acid;C06094;Q27103126;(1alpha,4aalpha,4bbeta,10beta)-7-hydroxy-1,4a-dimethyl-8-methylenegibbane-1,10-dicarboxylic acid;7alpha-hydroxy-1beta,4a-dimethyl-8-methylidene-4aalpha,4bbeta-gibbane-1alpha,10beta-dicarboxylic acid

Suppliers and Price of Gibberellin A53

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 2 raw suppliers

Chemical Property of Gibberellin A53

Chemical Property:

Vapor Pressure:1.05E-12mmHg at 25°C
Boiling Point:513.7°Cat760mmHg
Flash Point:278.6°C
PSA：94.83000
Density:1.3g/cm³
LogP:3.07560
XLogP3:2.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:348.19367399
Heavy Atom Count:25
Complexity:686

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC12CCCC(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)(C)C(=O)O
Isomeric SMILES:C[C@@]12CCC[C@@]([C@H]1[C@@H]([C@]34[C@H]2CC[C@](C3)(C(=C)C4)O)C(=O)O)(C)C(=O)O
Uses Gibberellin A53 is a derivative of the plant hormone Gibberellin which regulates growth and various developmental processes.

Technology Process of Gibberellin A53

There total 9 articles about Gibberellin A53 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: 71.0%

: 177781-09-8
C₂₂H₃₂O₆

: 51576-08-0
gibberellin A₅₃

Guidance literature:: With Dowex 50W-X₂ resin H⁽¹⁺⁾; water; In methanol; for 2h; Heating;

Reference yield:

: 29584-19-8,471-80-7
steviol

: 23313-48-6
gibberellin A₁₈

: 51576-05-7
7β-Hydroxysteviol

: 51576-08-0
gibberellin A₅₃

: 6β,7β-Dihydroxysteviol

Guidance literature:: With N,N,N-trimethyl-1-methyl-3-(3',3',5'-trimethylcyclohexyl)-2-propenyl-ammonium iodide; for 5h; Yield given. Further byproducts given. Yields of byproduct given; culture broth containing Gibberella fujikuroi, strain NRRL;

Reference yield:

: 29584-19-8,471-80-7
steviol

: 23313-48-6
gibberellin A₁₈

: 6980-44-5
gibberellin A₁₉

: 51576-05-7
7β-Hydroxysteviol

: 51576-08-0
gibberellin A₅₃

: 6β,7β-Dihydroxysteviol

: 545-97-1
gibberellin 1

Guidance literature:: With chlormequat chloride; for 120h; Product distribution; culture broth containing Gibberella fujikuroi, NRRL strain; other inhibitors of gibberellin biosynthesis, other times;