Obtusaquinone deriv jurd 1830

Base Information

Chemical Name:Obtusaquinone deriv jurd 1830
CAS No.:24126-88-3
Molecular Formula:C₁₆H₁₄O₃
Molecular Weight:254.285
Hs Code.:
NSC Number:269120
DSSTox Substance ID:DTXSID30421183
Mol file:24126-88-3.mol

Synonyms:NSC269120;24126-88-3;DTXSID30421183;NSC-269120;OBTUSAQUINONE DERIV JURD 1830

Suppliers and Price of Obtusaquinone deriv jurd 1830

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

Total 4 raw suppliers

Chemical Property of Obtusaquinone deriv jurd 1830

Chemical Property:

Vapor Pressure:1.95E-07mmHg at 25°C
Boiling Point:425.2°C at 760 mmHg
Flash Point:189.8°C
Density:1.18g/cm³
XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:254.094294304
Heavy Atom Count:19
Complexity:449

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=O)C(=CC1=O)CC=CC2=CC=CC=C2
Isomeric SMILES:COC1=CC(=O)C(=CC1=O)C/C=C/C2=CC=CC=C2

Technology Process of Obtusaquinone deriv jurd 1830

There total 4 articles about Obtusaquinone deriv jurd 1830 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:

: 4407-36-7
(2E)-3-phenyl-2-propen-1-ol

: 78889-17-5,24126-88-3
2-(trans-Cinnamyl)-5-methoxy-1,4-benzochinon

Guidance literature:: Multi-step reaction with 2 steps

1: ascorbic acid, citric acid / H₂O

2: Ag₂O / diethyl ether

With citric acid; silver(l) oxide; ascorbic acid; In diethyl ether; water;
DOI:10.1016/S0031-9422(00)86391-8

Reference yield:

: 24126-85-0
2-(trans-Cinnamyl)-5-methoxy-hydrochinon

: 78889-17-5,24126-88-3
2-(trans-Cinnamyl)-5-methoxy-1,4-benzochinon

Guidance literature:: With silver(l) oxide; In diethyl ether;
DOI:10.1016/0040-4020(78)88036-3 DOI:10.1016/S0031-9422(00)86391-8

Reference yield:

: 824-46-4
methoxyhydroquinone

: 78889-17-5,24126-88-3
2-(trans-Cinnamyl)-5-methoxy-1,4-benzochinon

Guidance literature:: Multi-step reaction with 2 steps

1: ascorbic acid, citric acid / H₂O

2: Ag₂O / diethyl ether

With citric acid; silver(l) oxide; ascorbic acid; In diethyl ether; water;
DOI:10.1016/S0031-9422(00)86391-8