Alloevodionol

Base Information

Chemical Name:Alloevodionol
CAS No.:484-18-4
Molecular Formula:C14H16O4
Molecular Weight:248.279
Hs Code.:
NSC Number:14135
DSSTox Substance ID:DTXSID30964060
Nikkaji Number:J12.491E
Wikidata:Q82945977
ChEMBL ID:CHEMBL1885077
Mol file:484-18-4.mol

Synonyms:ALLOEVODIONOL;484-18-4;NSC14135;Ethanone, 1-(7-hydroxy-5-methoxy-2,2-dimethyl-2H-1-benzopyran-8-yl)-;MLS002638354;1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone;Ketone, 7-hydroxy-5-methoxy-2,2-dimethyl-2H-1-benzopyran-8-yl methyl;allo-Evodionol;CHEMBL1885077;SCHEMBL21784054;DTXSID30964060;NSC-14135;SMR001547840;Ethanone,2-dimethyl-2H-1-benzopyran-8-yl)-;Ketone,2-dimethyl-2H-1-benzopyran-8-yl methyl;1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-chromen-8-yl)ethanone #;1-(7-Hydroxy-5-methoxy-2,2-dimethyl-2H-1-benzopyran-8-yl)ethan-1-one

Suppliers and Price of Alloevodionol

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 7 raw suppliers

Chemical Property of Alloevodionol

Chemical Property:

Vapor Pressure:8.16E-08mmHg at 25°C
Melting Point:71-72 °C
Boiling Point:424.7°Cat760mmHg
PKA:9.55±0.40(Predicted)
Flash Point:161°C
PSA：55.76000
Density:1.165g/cm³
LogP:2.78760
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:248.10485899
Heavy Atom Count:18
Complexity:361

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=C2C(=C(C=C1O)OC)C=CC(O2)(C)C

Technology Process of Alloevodionol

There total 5 articles about Alloevodionol 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: 95.0%

: 107-86-8
3,3-dimethyl acrylaldehyde

: 7507-89-3
2,6-dihydroxy-4-methoxy-acetophenone

: 484-18-4
1-(7-hydroxy-5-methoxy-2,2-dimethyl-2H-1-benzopyran-8-yl)-ethanone

Guidance literature:: With ethylenediamine diacetic acid; In xylene; for 10h; Heating;
DOI:10.1055/s-2007-990796

Reference yield:

: 4655-89-4
8-Acetyl-7-hydroxy-5-methoxy-3,4-dihydro-2,2-dimethyl-2H-<1>benzopyran

: 484-18-4
1-(7-hydroxy-5-methoxy-2,2-dimethyl-2H-1-benzopyran-8-yl)-ethanone

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In benzene; for 8h; Heating;

Reference yield:

: 7507-89-3
2,6-dihydroxy-4-methoxy-acetophenone

: 484-18-4
1-(7-hydroxy-5-methoxy-2,2-dimethyl-2H-1-benzopyran-8-yl)-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: 0.6 g / orthophosphoric acid / petroleum ether / 2 h / 30 - 35 °C

2: 0.065 g / DDQ / benzene / 8 h / Heating

With phosphoric acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In Petroleum ether; benzene;