7-Hydroxyflavanone

Base Information

Chemical Name:7-Hydroxyflavanone
CAS No.:6515-36-2
Molecular Formula:C15H12 O3
Molecular Weight:240.258
Hs Code.:2932999099
European Community (EC) Number:624-686-1
UNII:CC64495H41
DSSTox Substance ID:DTXSID0022430
Nikkaji Number:J502.873F
Wikidata:Q27116101
Metabolomics Workbench ID:75193
ChEMBL ID:CHEMBL97542
Mol file:6515-36-2.mol

Synonyms:7-hydroxyflavanone

Suppliers and Price of 7-Hydroxyflavanone

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

TRC
7-Hydroxyflavanone
50mg
$ 60.00

TRC
7-Hydroxyflavanone
25mg
$ 45.00

TRC
7-Hydroxyflavanone
250mg
$ 75.00

TCI Chemical
7-Hydroxyflavanone >98.0%(HPLC)(T)
5g
$ 141.00

TCI Chemical
7-Hydroxyflavanone >98.0%(HPLC)(T)
1g
$ 49.00

SynQuest Laboratories
7-Hydroxyflavanone 99%
1 g
$ 58.00

SynQuest Laboratories
7-Hydroxyflavanone 99%
25 g
$ 768.00

SynQuest Laboratories
7-Hydroxyflavanone 99%
5 g
$ 205.00

Sigma-Aldrich
7-Hydroxyflavanone 98%
5g
$ 229.00

Crysdot
7-Hydroxy-2-phenylchroman-4-one 95+%
25g
$ 588.00

Total 29 raw suppliers

Chemical Property of 7-Hydroxyflavanone

Chemical Property:

Appearance/Colour:Pale yellow crystalline powder
Vapor Pressure:3.05E-09mmHg at 25°C
Melting Point:188-190 °C(lit.)
Boiling Point:464.3°C at 760 mmHg
PKA:7.69±0.40(Predicted)
Flash Point:181.2°C
PSA：46.53000
Density:1.288g/cm³
LogP:3.09870
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:240.078644241
Heavy Atom Count:18
Complexity:309

Purity/Quality:

≥98% ^*data from raw suppliers

7-Hydroxyflavanone ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3
Uses 7-Hydroxyflavanone has been used for the stereoisomeric separation of flavonoids using polysaccharide-based chiral stationary phases by nano-liquid chromatography (nano-LC).

Technology Process of 7-Hydroxyflavanone

There total 33 articles about 7-Hydroxyflavanone 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%

: 1776-30-3
(E)-2',4'-dihydroxychalcone

: 6515-36-2,2545-13-3
7-hydroxy-2-phenyl-chroman-4-one

Guidance literature:: With potassium hydroxide; In methanol; at 25 ℃; for 4h;
DOI:10.1080/00397911.2016.1228110

Reference yield: 71.4%

: 126686-32-6
(E)-1-(2-hydroxy-4-(methoxymethoxy)phenyl)-3-phenylprop-2-en-1-one

: 1776-30-3
(E)-2',4'-dihydroxychalcone

: 6515-36-2,2545-13-3
7-hydroxy-2-phenyl-chroman-4-one

Guidance literature:: With hydrogenchloride; In methanol; at 100 ℃; for 2.5h;
DOI:10.1248/cpb.53.547

Reference yield: 70.0%

: 76240-27-2
7-hydroxy-2,3-dihydro-4H-chromen-4-one

: 98-80-6
phenylboronic acid

: 6515-36-2,2545-13-3
7-hydroxy-2-phenyl-chroman-4-one

Guidance literature:: 7-hydroxy-2,3-dihydro-4H-chromen-4-one; With [2,2]bipyridinyl; palladium(II) trifluoroacetate; oxygen; In 1,4-dioxane; dimethyl sulfoxide; at 100 ℃;

phenylboronic acid; With oxygen; trifluoroacetic acid; In 1,4-dioxane; dimethyl sulfoxide; at 80 ℃;
DOI:10.1021/acs.joc.9b01162