cis-(-)-Heptadeca-1,9-dien-4,6-diyn-3-ol

Base Information

Chemical Name:cis-(-)-Heptadeca-1,9-dien-4,6-diyn-3-ol
CAS No.:81203-57-8
Molecular Formula:C₁₇H₂₄O
Molecular Weight:244.377
Hs Code.:
Nikkaji Number:J1.106.214H,J935.487E
Wikipedia:Falcarinol
Mol file:81203-57-8.mol

Synonyms:falcarinol;falcarinol, (Z)-isomer;panaxynol

Suppliers and Price of cis-(-)-Heptadeca-1,9-dien-4,6-diyn-3-ol

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

Usbiological
Panaxynol
10mg
$ 546.00

TRC
Panaxynol
50mg
$ 680.00

TRC
Panaxynol
10mg
$ 165.00

Biorbyt Ltd
Panaxynol 95%
20 mg
$ 715.70

Biorbyt Ltd
Panaxynol 95%
10 mg
$ 596.70

Arctom
Panaxynol ≥98%
10mg
$ 388.00

Total 13 raw suppliers

Chemical Property of cis-(-)-Heptadeca-1,9-dien-4,6-diyn-3-ol

Chemical Property:

Vapor Pressure:5.3E-07mmHg at 25°C
Boiling Point:370.6°C at 760 mmHg
PKA:11.66±0.20(Predicted)
Flash Point:163.4°C
PSA：20.23000
Density:0.931g/cm³
LogP:3.84690
XLogP3:5.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:9
Exact Mass:244.182715385
Heavy Atom Count:18
Complexity:363

Purity/Quality:

Analysis control,HPLC≥98% ^*data from raw suppliers

Panaxynol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Biological Agents -> Plant Toxins
Canonical SMILES:CCCCCCCC=CCC#CC#CC(C=C)O
Isomeric SMILES:CCCCCCC/C=C/CC#CC#CC(C=C)O
Uses Panaxynol is derived from 2-Decyn-1-ol (D228475), which is used in the synthesis of anti-tumor agents, isomers of Panaxytriol and Falcarinol (F101100). Also used in the synthesis of aromatase inhibitors used in the treatment of cancers, primarily breast and ovarian; Anti-diabetic agent.

Technology Process of cis-(-)-Heptadeca-1,9-dien-4,6-diyn-3-ol

There total 15 articles about cis-(-)-Heptadeca-1,9-dien-4,6-diyn-3-ol 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: 85.0%

: 223558-75-6
tert-Butyl-diphenyl-((Z)-(S)-1-vinyl-pentadec-7-ene-2,4-diynyloxy)-silane

: 81203-57-8
(3S,9Z)-1,9-heptadecadiene-4,6-diyn-3-ol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; Ambient temperature;
DOI:10.1016/S0040-4039(99)00224-5

Reference yield: 73.0%

: 135457-18-0
(Z)-1-chlorodec-2-ene

: 405144-93-6
(3S)-hept-1-ene-4,6-diyn-3-ol

: 81203-57-8
(3S,9Z)-1,9-heptadecadiene-4,6-diyn-3-ol

Guidance literature:: (3S)-hept-1-ene-4,6-diyn-3-ol; With copper(l) iodide; tetrabutyl-ammonium chloride; potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h;

(Z)-1-chlorodec-2-ene; In N,N-dimethyl-formamide; at 20 ℃; for 7h; Further stages.;
DOI:10.1021/jo020073w

Reference yield: 49.0%

: 108-05-4,9003-20-7
vinyl acetate

: 4117-12-8
panaxynol

: 146396-38-5
(R)-acetoxyfalcarinol

: 81203-57-8
(3S,9Z)-1,9-heptadecadiene-4,6-diyn-3-ol

Guidance literature:: With immobilised Candida antarctica lipase B; In di-isopropyl ether; at 20 ℃; for 30h; optical yield given as %ee; enantioselective reaction; Enzymatic reaction;
DOI:10.1016/j.tet.2010.10.049