Gibberellin A63

Base Information

Chemical Name:Gibberellin A63
CAS No.:63351-80-4
Molecular Formula:C19H24O6
Molecular Weight:348.39
Hs Code.:
DSSTox Substance ID:DTXSID401108576
Nikkaji Number:J147.243G
Wikidata:Q105240620

Synonyms:Gibberellin A63;GA63;CHEBI:142004;DTXSID401108576;(1S,2S,4aR,4bR,7R,9R,9aR,10S,10aR)-2,9-dihydroxy-1-methyl-8-methylene-13-oxododecahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid;(1S,2S,4aR,4bR,7R,9R,9aR,10S,10aR)-2,9-dihydroxy-1-methyl-8-methylidene-13-oxododecahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid;2beta,9beta-dihydroxy-1beta-methyl-8-methylidene-13-oxo-4a,1alpha-epoxymethano-4aalpha,4bbeta-gibbane-10beta-carboxylic acid;Gibbane-1,10-dicarboxylic acid, 2,4a,9-trihydroxy-1-methyl-8-methylene-, 1,4a-lactone, (1alpha,2beta,4aalpha,4bbeta,9beta,10beta)-

Suppliers and Price of Gibberellin A63

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

TRC
GibberellinA63
10mg
$ 1540.00

Total 0 raw suppliers

Chemical Property of Gibberellin A63

Chemical Property:

PSA：104.06000
LogP:1.10700
XLogP3:0.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:1
Exact Mass:348.15728848
Heavy Atom Count:25
Complexity:717

Purity/Quality:: GibberellinA63 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5O)C(=O)O)OC2=O)O
Isomeric SMILES:C[C@@]12[C@H](CC[C@@]3([C@@H]1[C@@H]([C@]45[C@H]3CC[C@H](C4)C(=C)[C@H]5O)C(=O)O)OC2=O)O
Uses Gibberellin A63 is a derivative of Gibberellic Acid (G377450), a hormone that is found in plants which promotes the growth and elongation of cells. Gibberellic acid acts as a plant growth regulator on account of its physiological and morphological effects in extremely low concentrations.

Technology Process of Gibberellin A63

There total 6 articles about Gibberellin A63 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:

: 97344-17-7
15β-hydroxy GA₄ 3-acetate

: 63351-80-4
ent-3α,10,15α-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 19,10-lactone

Guidance literature:: With potassium carbonate; In methanol; for 12h; Heating;

Reference yield:

: 468-44-0
gibberellin A₄

: 63351-80-4
ent-3α,10,15α-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 19,10-lactone

Guidance literature:: Multi-step reaction with 6 steps

1: KHCO₃, 18-crown-6 / acetonitrile / 1 h / Heating

2: pyridine / 2 h

3: SeO₂, t-butylhydroperoxide / CH₂Cl₂ / 2 h

4: COCl₂, DMSO / CH₂Cl₂ / 1 h / -72 - -60 °C

5: Zn / acetic acid / 1 h / Ambient temperature

6: K₂CO₃ / methanol / 12 h / Heating

With tert.-butylhydroperoxide; selenium(IV) oxide; 18-crown-6 ether; potassium carbonate; potassium hydrogencarbonate; dimethyl sulfoxide; zinc; In pyridine; methanol; dichloromethane; acetic acid; acetonitrile;

Reference yield:

: 79368-09-5
GA₄ phenacyl ester

: 63351-80-4
ent-3α,10,15α-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 19,10-lactone

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine / 2 h

2: SeO₂, t-butylhydroperoxide / CH₂Cl₂ / 2 h

3: COCl₂, DMSO / CH₂Cl₂ / 1 h / -72 - -60 °C

4: Zn / acetic acid / 1 h / Ambient temperature

5: K₂CO₃ / methanol / 12 h / Heating

With tert.-butylhydroperoxide; selenium(IV) oxide; potassium carbonate; dimethyl sulfoxide; zinc; In pyridine; methanol; dichloromethane; acetic acid;