Gibberellin A8

Base Information

Chemical Name:Gibberellin A8
CAS No.:7044-72-6
Molecular Formula:C19H24O7
Molecular Weight:364.38966
Hs Code.:
European Community (EC) Number:829-307-5
DSSTox Substance ID:DTXSID70990646
Nikkaji Number:J4.745G
Wikidata:Q27103931
Mol file:7044-72-6.mol

Synonyms:Gibberellin A8;7044-72-6;(1R,2R,5S,8S,9S,10R,11S,12R,13S)-5,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid;2beta-Hydroxygibberellin 1;3beta-hydroxygibberellin A1;SCHEMBL8495837;CHEBI:28861;DTXSID70990646;GA8;Q27103931;(1R,2R,5S,8S,9S,10R,11S,12R,13S)-5,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1(5,8).0(1,10).0(2,8)]heptadecane-9-carboxylic acid;2beta,3beta,7alpha-trihydroxy-1beta-methyl-8-methylidene-13-oxo-4a,1alpha-epoxymethano-4aalpha,4bbeta-gibbane-10beta-carboxylic acid;Gibbane-1,10-dicarboxylic acid, 2,3,4a,7-tetrahydroxy-1-methyl-8-methylene-, 1,4a-lactone, (1.alpha.,2.beta.,3.beta.,4a.alpha.,4b.beta.,10.beta.)-

Suppliers and Price of Gibberellin A8

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
GibberellinA8
10mg
$ 1390.00

TRC
GibberellinA8
1mg
$ 180.00

Total 8 raw suppliers

Chemical Property of Gibberellin A8

Chemical Property:

Vapor Pressure:6.55E-19mmHg at 25°C
Melting Point:>140°C
Boiling Point:637.1°C at 760 mmHg
Flash Point:232.3°C
PSA：124.29000
Density:1.54g/cm³
LogP:0.22190
Storage Temp.:Amber Vial, -20°C Freezer, Under inert atmosphere
Solubility.:DMSO (Slightly), Ethanol (Slightly, Sonicated)
XLogP3:-0.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:1
Exact Mass:364.15220310
Heavy Atom Count:26
Complexity:763

Purity/Quality:

98% ^*data from raw suppliers

GibberellinA8 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC12C3C(C45CC(=C)C(C4)(CCC5C3(CC(C1O)O)OC2=O)O)C(=O)O
Isomeric SMILES:C[C@]12[C@H]3[C@@H]([C@@]45CC(=C)[C@@](C4)(CC[C@H]5[C@@]3(C[C@@H]([C@@H]1O)O)OC2=O)O)C(=O)O
Uses Gibberellin A8 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 A8

There total 5 articles about Gibberellin A8 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: 95.5%

: 170512-93-3
C₂₇H₂₉BrO₈

: 7044-72-6,72533-76-7
Gibberellin-A(8)

Guidance literature:: With ammonium chloride; acetic acid; zinc; In methanol; for 2h;
DOI:10.1007/BF00629875

Reference yield:

: 77-06-5
(3S,3aS,4S,4aS,6S,8aR,8bR,11S)-6,11-dihydroxy-3-methyl-12-methylene-2-oxo-4a,6-ethano-3,8b-prop-1-enoperhydroindeno[1,2-b]furan-4-carboxylic acid

: 7044-72-6,72533-76-7
Gibberellin-A(8)

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) aq. Na₂CO₃, 2.) Et₃N / 1.) 96 deg C, 6 h, 2.) acetone, RT, 12 h

2: 79.6 percent / 2,2-azobis(2-methylpropionitrile), (n-Bu)3SnH / tetrahydrofuran; benzene / 0.42 h / 70 °C

3: 95.5 percent / Zn, NH₄Cl, AcOH / methanol / 2 h

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; sodium carbonate; ammonium chloride; acetic acid; triethylamine; zinc; In tetrahydrofuran; methanol; benzene;
DOI:10.1007/BF00629875

Reference yield:

: 170512-92-2
C₂₇H₂₈BrIO₈

: 7044-72-6,72533-76-7
Gibberellin-A(8)

Guidance literature:: Multi-step reaction with 2 steps

1: 79.6 percent / 2,2-azobis(2-methylpropionitrile), (n-Bu)3SnH / tetrahydrofuran; benzene / 0.42 h / 70 °C

2: 95.5 percent / Zn, NH₄Cl, AcOH / methanol / 2 h

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; ammonium chloride; acetic acid; zinc; In tetrahydrofuran; methanol; benzene;
DOI:10.1007/BF00629875