(2S)-7-hydroxyflavanone

Base Information

Chemical Name:(2S)-7-hydroxyflavanone
CAS No.:2545-13-3
Molecular Formula:C₁₅H₁₂O₃
Molecular Weight:240.258
Hs Code.:
UNII:MF98742K2H
DSSTox Substance ID:DTXSID90350985
Nikkaji Number:J641.665I
Wikidata:Q27095092
Metabolomics Workbench ID:56435
ChEMBL ID:CHEMBL402744
Mol file:2545-13-3.mol

Synonyms:(2S)-7-hydroxyflavanone;7-hydroxy-2-phenyl-chroman-4-one;5,4'-DIDEOXYFLAVANONE;(-)-7-Hydroxyflavanone;2545-13-3;(2S)-7-hydroxy-2-phenyl-2,3-dihydro-4H-chromen-4-one;(S)-7-Hydroxy-2-phenylchroman-4-one;CHEBI:41888;7-Hydroxyflavanone, (S)-;(2S)-7-hydroxy-2-phenyl-2,3-dihydrochromen-4-one;J641.665I;CHEMBL402744;Flavanone, 7-hydroxy-, (-)-;MF98742K2H;4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-phenyl-, (S)-;4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-phenyl-, (2S)-;2H-1-Benzopyran-7-yloxy;(S)-7-hydroxyflavanone;BIDD:ER0186;UNII-MF98742K2H;SCHEMBL1072683;DTXSID90350985;BDBM50535254;DB04274;Q27095092

Suppliers and Price of (2S)-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

Sigma-Aldrich
7-Hydroxyflavanone 98%
5 g
$ 205.00

AHH
7-Hydroxyflavanone 98%
25g
$ 558.00

Total 5 raw suppliers

Chemical Property of (2S)-7-hydroxyflavanone

Chemical Property:

PSA：46.53000
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:

99% ^*data from raw suppliers

7-Hydroxyflavanone 98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3
Isomeric SMILES:C1[C@H](OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3

Technology Process of (2S)-7-hydroxyflavanone

There total 41 articles about (2S)-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: 88.0%

: 126686-33-7
(S)-2,3-dihydro-7-(methoxymethoxy)-2-phenyl-4H-1-benzopyran-4-one

: 2545-13-3
(S)-2,3-dihydro-7-hydroxy-2-phenyl-4H-1-benzopyran-4-one

Guidance literature:: With hydrogenchloride; water; In dichloromethane; at 20 ℃; for 96h;
DOI:10.1021/ol2004148

Reference yield: 77.0%

: 59887-89-7
7-hydroxy-4H-chromen-4-one

: 98-80-6
phenylboronic acid

: 41680-08-4,2545-13-3
(R)-7-hydroxy-2-phenylchroman-4-one

Guidance literature:: phenylboronic acid; With ammonium hexafluorophosphate; palladium(II) trifluoroacetate; 2-[(S)-4,5-dihydro-4-tert-butyl-1,3-oxazol-2-yl]pyridine; In 1,2-dichloro-ethane; at 20 ℃;

7-hydroxy-4H-chromen-4-one; In water; 1,2-dichloro-ethane; at 60 ℃; for 12h; enantioselective reaction;
DOI:10.1002/chem.201203643