Gibberellin A14

Base Information

Chemical Name:Gibberellin A14
CAS No.:4955-22-0
Molecular Formula:C20H28O5
Molecular Weight:348.43
Hs Code.:
DSSTox Substance ID:DTXSID90332089
Nikkaji Number:J8.619C
Wikidata:Q27110160
Metabolomics Workbench ID:28571
Mol file:4955-22-0.mol

Synonyms:Gibberellin A14;4955-22-0;(1R,2S,3S,4S,5S,8S,9S,12R)-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid;429678-85-3;gibberellin 14;GA14;SCHEMBL16499754;CHEBI:29588;DTXSID90332089;AKOS040734846;LMPR0104170015;NCGC00380833-01;ent-3alpha-hydroxygibberell-16-ene-7,9-dioic acid;Q27110160;(1R,2S,3S,4S,5S,8S,9S,12R)-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.0(1,9).0(3,8)]pentadecane-2,4-dicarboxylic acid;2beta-hydroxy-1beta,4a-dimethyl-8-methylidene-4aalpha,4bbeta-gibbane-1alpha,10beta-dicarboxylic acid;NCGC00380833-01_C20H28O5_Gibbane-1,10-dicarboxylic acid, 2-hydroxy-1,4a-dimethyl-8-methylene-, (1alpha,2beta,4aalpha,4bbeta,10beta)-

Suppliers and Price of Gibberellin A14

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Gibberellin A14

Chemical Property:

Vapor Pressure:7.71E-13mmHg at 25°C
Boiling Point:516.7°C at 760 mmHg
Flash Point:280.4°C
Density:1.3g/cm³
XLogP3:3.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:348.19367399
Heavy Atom Count:25
Complexity:671

Purity/Quality:

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MSDS Files:

Useful:

Canonical SMILES:CC12CCC(C(C1C(C34C2CCC(C3)C(=C)C4)C(=O)O)(C)C(=O)O)O
Isomeric SMILES:C[C@@]12CC[C@@H]([C@@]([C@H]1[C@@H]([C@]34[C@H]2CC[C@H](C3)C(=C)C4)C(=O)O)(C)C(=O)O)O
Uses Giberellin A14 is a regulatory molecule in plant growth and development. Giberellins are responsible for cell growth and elongation and can even affect gene transcription levels.

Technology Process of Gibberellin A14

There total 1 articles about Gibberellin A14 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: