Euphorbadienol

Base Information

Chemical Name:Euphorbadienol
CAS No.:566-14-3
Deprecated CAS:23299-38-9
Molecular Formula:C₃₁H₅₂O
Molecular Weight:440.753
Hs Code.:
Nikkaji Number:J14.837G
Wikidata:Q105329031
Metabolomics Workbench ID:141751
ChEMBL ID:CHEMBL518556
Mol file:566-14-3.mol

Synonyms:24-methylenelanost-8-en-3 beta-ol;ebericol;ebericol, (14)C-labeled;eburicol;euphorbol

Suppliers and Price of Euphorbadienol

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

Biosynth Carbosynth
alpha-Euphorbol
25 mg
$ 1250.00

Biosynth Carbosynth
alpha-Euphorbol
10 mg
$ 600.00

Biosynth Carbosynth
alpha-Euphorbol
5 mg
$ 325.00

Biosynth Carbosynth
alpha-Euphorbol
2 mg
$ 150.00

Biosynth Carbosynth
alpha-Euphorbol
1 mg
$ 100.00

Total 15 raw suppliers

Chemical Property of Euphorbadienol

Chemical Property:

Vapor Pressure:2.25E-12mmHg at 25°C
Boiling Point:506.4°C at 760 mmHg
Flash Point:225.7°C
PSA：20.23000
Density:0.97g/cm³
LogP:8.72510
XLogP3:9.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:440.401816278
Heavy Atom Count:32
Complexity:786

Purity/Quality:

99% ^*data from raw suppliers

alpha-Euphorbol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C
Isomeric SMILES:C[C@@H](CCC(=C)C(C)C)[C@@H]1CC[C@]2([C@]1(CCC3=C2CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C
Use Description Euphorbol, which likely refers to compounds derived from the Euphorbia plant family, has several applications across different fields. In traditional medicine and ethnobotany, some Euphorbia species have been used for their medicinal properties, such as pain relief and treatment of skin conditions. In the field of agriculture, certain Euphorbia plants are considered weeds and can have economic significance as invasive species that impact crop yield and land use. In the realm of horticulture, some ornamental Euphorbia species are cultivated for their unique and exotic appearance in gardens and landscaping. Additionally, in botany and plant taxonomy, Euphorbia species play a role as subjects of study for understanding plant diversity and classification. However, it's crucial to note that some Euphorbia species contain toxic compounds, and their usage should be approached with caution, with proper knowledge of their specific properties and potential hazards.

Technology Process of Euphorbadienol

There total 10 articles about Euphorbadienol 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: 55.0%

: 79-63-0
tirucallol

: 516-28-9,566-14-3,97719-41-0,6890-88-6
24-methylenelanost-8-en-3-ol

Guidance literature:: With Paracoccidiodes brasiliensis sterol C₂₄-methyltransferase, recombinant; AdoMet; Enzymatic reaction;
DOI:10.1016/j.bbalip.2010.06.007

Reference yield:

: 14787-39-4,17837-80-8
3β-acetoxy-24-methylene-lanost-8-ene

: 516-28-9,566-14-3,97719-41-0,6890-88-6
24-methylenelanost-8-en-3-ol

Guidance literature:: With sodium methylate; In methanol; for 1h; Heating;
DOI:10.1016/0031-9422(81)80020-9

Reference yield:

: 13879-13-5,54325-09-6,5539-04-8
lanosta-8,24-dien-3-one

: 516-28-9,566-14-3,97719-41-0,6890-88-6
24-methylenelanost-8-en-3-ol

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / ethylene glycol / 5 h / Reflux

2: recombinant Paracoccidioides brasiliensis sterol C₂₄-methyltransferase cell lysate / glycerol / 1 h / 35 °C / pH 8 / aq. phosphate buffer

With potassium hydroxide; In ethylene glycol; glycerol;
DOI:10.1016/j.abb.2012.03.002