Cudraflavanone B

Base Information

Chemical Name:Cudraflavanone B
CAS No.:597542-74-0
Molecular Formula:C₂₀H₂₀O₆
Molecular Weight:356.375
Hs Code.:

Synonyms:

Suppliers and Price of Cudraflavanone B

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

Arctom
CudraflavanoneB ≥98%
5mg
$ 468.00

Total 9 raw suppliers

Chemical Property of Cudraflavanone B

Chemical Property:

Purity/Quality:

99%+, ^*data from raw suppliers

CudraflavanoneB ≥98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Cudraflavanone B

There total 2 articles about Cudraflavanone B 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:

: 780724-90-5
dimethylallyl diphosphate

: 56486-94-3
(2S)-2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one

: 1049662-29-4,97938-30-2
sophoraflavone G

: 152464-78-3
8-dimethylallylsteppogenin

: 597542-74-0
6-dimethylallyl-2'-hydroxynaringenin

Guidance literature:: With naringenin 8-dimethylallyltransferase; magnesium chloride; In ethanol; water; at 25 ℃; pH=7.5 - 9; Enzymatic reaction;
DOI:10.1016/S0031-9422(00)00198-9

Reference yield:

: 358-72-5
dimethylallyl diphosphate

: 56486-94-3
(2S)-2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one

: 152464-78-3
8-dimethylallylsteppogenin

: 597542-74-0
6-dimethylallyl-2'-hydroxynaringenin

Guidance literature:: With recombinant Sophora flavescens flavonoid prenyltransferase; magnesium chloride; In aq. buffer; at 40 ℃; for 2h; pH=9; Overall yield = 29.9 %; stereospecific reaction; Kinetics; Enzymatic reaction;
DOI:10.1002/adsc.201300196