4H-1-Benzopyran-4-one, 2-(4-(beta-D-glucopyranosyloxy)phenyl)-2,3-dihy dro-5,7-dihydroxy-, (2S)-

Base Information

Chemical Name:4H-1-Benzopyran-4-one, 2-(4-(beta-D-glucopyranosyloxy)phenyl)-2,3-dihy dro-5,7-dihydroxy-, (2S)-
CAS No.:81202-36-0
Molecular Formula:C₂₁H₂₂O₁₀
Molecular Weight:434.4
Hs Code.:
Mol file:81202-36-0.mol

Synonyms:4H-1-Benzopyran-4-one,2-[4-(b-D-glucopyranosyloxy)phenyl]-2,3-dihydro-5,7-dihydroxy-,(S)-; 5-Hydroxyliquiritin; Choerospondin; Naringenin 4'-O-b-D-glucopyranoside; Naringenin4'-glucoside

Suppliers and Price of 4H-1-Benzopyran-4-one, 2-(4-(beta-D-glucopyranosyloxy)phenyl)-2,3-dihy dro-5,7-dihydroxy-, (2S)-

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

ChemScene
Choerospondin 99.62%
5mg
$ 790.00

Total 12 raw suppliers

Chemical Property of 4H-1-Benzopyran-4-one, 2-(4-(beta-D-glucopyranosyloxy)phenyl)-2,3-dihy dro-5,7-dihydroxy-, (2S)-

Chemical Property:

Vapor Pressure:1.14E-25mmHg at 25°C
Melting Point:191 °C
Boiling Point:780.8°C at 760 mmHg
PKA:7.50±0.40(Predicted)
Flash Point:276.9°C
PSA：166.14000
Density:1.597g/cm³
LogP:-0.01700

Purity/Quality:

HPLC≥98% ^*data from raw suppliers

Choerospondin 99.62% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4H-1-Benzopyran-4-one, 2-(4-(beta-D-glucopyranosyloxy)phenyl)-2,3-dihy dro-5,7-dihydroxy-, (2S)-

There total 6 articles about 4H-1-Benzopyran-4-one, 2-(4-(beta-D-glucopyranosyloxy)phenyl)-2,3-dihy dro-5,7-dihydroxy-, (2S)- 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: 96.6%

: naringenin 4'-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside)

: 81202-36-0
naringenin 4′-O-β-D-glucopyranoside

Guidance literature:: With sodium methylate; In methanol; at 0 ℃; for 1h;
DOI:10.1271/bbb.58.1479

Reference yield:

: 551-15-5
liquiritin

: 2196-14-7
7,4'-Dihydroxyflavon

: 520-36-5
5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

: C₂₁H₂₂O₁₀

: C₂₁H₂₂O₁₀

: C₂₁H₂₂O₁₀

: 578-86-9,41680-09-5
liquiritigenin

: 22052-75-1
kumatakenin B-4'-O-glucoside

: 81202-36-0
naringenin 4′-O-β-D-glucopyranoside

Guidance literature:: With glucose-6-phosphate dehydrogenase; α-D-glucose 6-phosphate; NADPH; magnesium chloride; In methanol; aq. phosphate buffer; at 37 ℃; for 0.583333h; Microbiological reaction; Enzymatic reaction;
DOI:10.1039/c7ra13760e

Reference yield:

: 133-89-1
UDP-glucose

: 480-41-1
naringenin

: 1211464-47-9
(2S)-naringenin-7,4′-di-O-β-D-glucopyranoside

: 529-55-5,88275-21-2,127469-97-0
prunin

: 81202-36-0
naringenin 4′-O-β-D-glucopyranoside

Guidance literature:: With glycosyltransferases YdhE bacillus licheniformi; magnesium chloride; In dimethyl sulfoxide; at 30 ℃; for 3h; pH=8.8; Enzymatic reaction;
DOI:10.1021/acs.orglett.9b03040