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(+)-[2-[2,6-Dihydroxy-4-(6-hydroxybenzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methyl-3-cyclohexen-1-yl][2,4-dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]methanone is a complex organic molecule characterized by a cyclohexenyl and phenyl ring structure. It features multiple hydroxyl groups and a ketone functional group, which may contribute to its potential antioxidant properties. The presence of a benzofuran-2-yl and a buten-1-yl group suggests that (+)-[2-[2,6-Dihydroxy-4-(6-hydroxybenzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methyl-3-cyclohexen-1-yl][2,4-dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]methanone could have pharmaceutical or biological activity. Further research is required to explore its full potential and applications.

76472-89-4

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76472-89-4 Usage

Uses

Used in Pharmaceutical Industry:
(+)-[2-[2,6-Dihydroxy-4-(6-hydroxybenzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methyl-3-cyclohexen-1-yl][2,4-dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]methanone is used as a potential pharmaceutical agent for its possible antioxidant properties and biological activity. The presence of multiple hydroxyl groups and the benzofuran-2-yl and buten-1-yl groups may contribute to its efficacy in treating various conditions or diseases.
Used in Cosmetic Industry:
In the cosmetic industry, (+)-[2-[2,6-Dihydroxy-4-(6-hydroxybenzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methyl-3-cyclohexen-1-yl][2,4-dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]methanone may be utilized for its antioxidant properties, which could help protect the skin from oxidative stress and environmental damage, thus promoting skin health and appearance.
Used in Research and Development:
(+)-[2-[2,6-Dihydroxy-4-(6-hydroxybenzofuran-2-yl)phenyl]-6-(2,4-dihydroxyphenyl)-4-methyl-3-cyclohexen-1-yl][2,4-dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]methanone is used as a subject of research and development for its complex structure and potential properties. Scientists and researchers may investigate its chemical behavior, interactions with biological systems, and possible applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 76472-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76472-89:
(7*7)+(6*6)+(5*4)+(4*7)+(3*2)+(2*8)+(1*9)=164
164 % 10 = 4
So 76472-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C39H36O9/c1-19(2)4-8-27-30(42)11-10-28(38(27)46)39(47)29-13-23(12-20(3)36(29)26-9-7-24(40)17-31(26)43)37-32(44)14-22(15-33(37)45)34-16-21-5-6-25(41)18-35(21)48-34/h4-7,9-12,14-18,23,29,36,40-46H,8,13H2,1-3H3/t23-,29-,36+/m1/s1

76472-89-4SDS

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 [(1R,2S,5S)-5-[2,6-dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-2-(2,4-dihydroxyphenyl)-3-methylcyclohex-3-en-1-yl]-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]methanone

1.2 Other means of identification

Product number -
Other names calcomoracin

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:76472-89-4 SDS

76472-89-4Upstream product

76472-89-4Relevant academic research and scientific papers

Dual p-coumaroyl CoA biosynthesis in Morus alba cell cultures

Hano, Yoshio,Shimazaki, Manabu,Nomura, Taro,Ueda, Shinichi

, p. 989 - 994 (2007/10/03)

Morus alba callus and cell suspension cultures specifically produce chalcomoracin (1) and kuwanon J (2) both originated from cinnamoylpolyketide intermediate. Administration of [2-13C]cinnamic acid N-acetylcysteamine thioester to the M. alba ce

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