4aalpha,4bbeta-Gibbane-1alpha,4a,10beta-tricarboxylic acid, 2beta-hydr oxy-1-methyl-8-methylene-, trimethyl ester

Base Information

Chemical Name:4aalpha,4bbeta-Gibbane-1alpha,4a,10beta-tricarboxylic acid, 2beta-hydr oxy-1-methyl-8-methylene-, trimethyl ester
CAS No.:22882-63-9
Molecular Formula:C₂₃H₃₂O₇
Molecular Weight:420.503
Hs Code.:
Mol file:22882-63-9.mol

Synonyms:4aa,4bb-Gibbane-1a,4a,10b-tricarboxylic acid, 2b-hydroxy-1-methyl-8-methylene-,trimethyl ester (8CI); Gibberellin A13 trimethyl ester (7CI);4aH-7,9a-Methanobenz[a]azulene, gibbane-1,4a,10-tricarboxylic acid deriv.; GA13trimethyl ester

Suppliers and Price of 4aalpha,4bbeta-Gibbane-1alpha,4a,10beta-tricarboxylic acid, 2beta-hydr oxy-1-methyl-8-methylene-, trimethyl ester

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

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Chemical Property of 4aalpha,4bbeta-Gibbane-1alpha,4a,10beta-tricarboxylic acid, 2beta-hydr oxy-1-methyl-8-methylene-, trimethyl ester

Chemical Property:

PSA：99.13000
LogP:2.26140

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4aalpha,4bbeta-Gibbane-1alpha,4a,10beta-tricarboxylic acid, 2beta-hydr oxy-1-methyl-8-methylene-, trimethyl ester

There total 14 articles about 4aalpha,4bbeta-Gibbane-1alpha,4a,10beta-tricarboxylic acid, 2beta-hydr oxy-1-methyl-8-methylene-, trimethyl ester 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:

: 38076-27-6
ent-3α-acetoxygibberell-16-ene-7,19,20-trioic acid 7,19-dimethyl ester

: 22882-63-9,55873-60-4,106202-99-7
y-Hydroxy-GA⁽²⁵⁾-methylester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / tetrahydrofuran / 7 h / Ambient temperature

2: 55 mg / methanol / 163 h

With triethylamine; In tetrahydrofuran; methanol;

Reference yield:

: 106202-95-3
C₂₃H₃₀O₈

: 22882-63-9,55873-60-4,106202-99-7
6-epi-gibberellin A13 trimethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 350 mg / toluene-p-sulphonyl chloride, Et₃N / tetrahydrofuran / 17 h / Ambient temperature

2: 65 mg / KOH-CH₃OH / CHCl₃ / 2.5 h / Ambient temperature

With potassium hydroxide; triethylamine; p-toluenesulfonyl chloride; In tetrahydrofuran; chloroform;

Reference yield:

: 3467-04-7
C₂₂H₂₆O₇

: 22882-63-9,55873-60-4,106202-99-7
6-epi-gibberellin A13 trimethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 40 h / Heating

2: 350 mg / toluene-p-sulphonyl chloride, Et₃N / tetrahydrofuran / 17 h / Ambient temperature

3: 65 mg / KOH-CH₃OH / CHCl₃ / 2.5 h / Ambient temperature

With potassium hydroxide; triethylamine; p-toluenesulfonyl chloride; In tetrahydrofuran; chloroform;