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(2S)-5,7-Dihydroxy-2,3-dihydro-2α-[[(2R)-2β-(4-hydroxyphenyl)-3α-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydrobenzofuran]-5-yl]-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one is a complex flavonoid molecule with a benzopyran backbone and multiple hydroxyl groups. It has a chiral center at the 2-position and a side chain containing a 3-methyl-2-butenyl group. (2S)-5,7-Dihydroxy-2,3-dihydro-2α-[[(2R)-2β-(4-hydroxyphenyl)-3α-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydrobenzofuran]-5-yl]-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one also contains a biphenyl substructure with hydroxyphenyl groups at the 4and 6-positions. The intricate structure of this chemical suggests potential biological activity, possibly as an antioxidant or anti-inflammatory agent, due to the presence of multiple hydroxyl groups and aromatic rings.

136997-68-7

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136997-68-7 Usage

Uses

Used in Pharmaceutical Industry:
(2S)-5,7-Dihydroxy-2,3-dihydro-2α-[[(2R)-2β-(4-hydroxyphenyl)-3α-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydrobenzofuran]-5-yl]-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one is used as a potential antioxidant or anti-inflammatory agent for its possible biological activity due to the presence of multiple hydroxyl groups and aromatic rings.
Used in Nutraceutical Industry:
(2S)-5,7-Dihydroxy-2,3-dihydro-2α-[[(2R)-2β-(4-hydroxyphenyl)-3α-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydrobenzofuran]-5-yl]-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one is used as a dietary supplement for its potential health benefits as an antioxidant or anti-inflammatory agent.
Used in Cosmetic Industry:
(2S)-5,7-Dihydroxy-2,3-dihydro-2α-[[(2R)-2β-(4-hydroxyphenyl)-3α-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydrobenzofuran]-5-yl]-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one is used as an ingredient in skincare products for its potential antioxidant and anti-inflammatory properties.
Note: The uses listed above are speculative based on the chemical structure and potential biological activity of the compound. Further research is needed to fully understand the pharmacological properties and potential applications of (2S)-5,7-Dihydroxy-2,3-dihydro-2α-[[(2R)-2β-(4-hydroxyphenyl)-3α-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydrobenzofuran]-5-yl]-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one.

Check Digit Verification of cas no

The CAS Registry Mumber 136997-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,9,9 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136997-68:
(8*1)+(7*3)+(6*6)+(5*9)+(4*9)+(3*7)+(2*6)+(1*8)=187
187 % 10 = 7
So 136997-68-7 is a valid CAS Registry Number.

136997-68-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Sophoraflavanone H

1.2 Other means of identification

Product number -
Other names sophoraflavanone H

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:136997-68-7 SDS

136997-68-7Downstream Products

136997-68-7Relevant academic research and scientific papers

Total Synthesis of Sophoraflavanone H and Confirmation of Its Absolute Configuration

Asakawa, Tomohiro,Egi, Masahiro,Hiza, Aiki,Inai, Makoto,Ishikawa, Ryo,Ishikawa, Yoshinobu,Kan, Toshiyuki,Kondo, Mitsuru,Murakami, Haruka,Muramatsu, Yoshihiro,Ouchi, Hitoshi,Taniguchi, Tohru,Tokumaru, Yohei,Tsukaguchi, Yuta,Yoshimura, Fumihiko

, (2020/05/25)

Sophoraflavanone H (1) is a polyphenol with a hybrid-type structure containing 2,3-diaryl-2,3-dihydrobenzofuran and flavanone ring moieties. This compound and related analogues are promising leads for antimicrobial and antitumor drug development. Here we

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