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CAS

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93993-77-2

(2E)-1-(3,6-dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one, commonly known as dihydromorin, is a naturally occurring chalcone derivative found in the roots of plants in the Morus genus. (2E)-1-(3,6-dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one possesses potential antioxidant and anti-inflammatory properties, making it a subject of interest for its potential health benefits and medicinal applications.
Used in Pharmaceutical Industry:
Dihydromorin is used as a potential cancer treatment agent for its inhibitory effects on the growth of cancer cells. It has demonstrated the ability to target various types of cancer, offering a promising avenue for therapeutic intervention.
Used in Diabetes Treatment:
In the medical field, dihydromorin is used as a potential treatment for diabetes due to its capacity to help regulate glucose metabolism, which can contribute to better disease management and improved patient outcomes.
Overall, (2E)-1-(3,6-dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one, or dihydromorin, is a chemical compound with significant potential in both the pharmaceutical and medical industries, particularly for cancer treatment and diabetes management. Its antioxidant and anti-inflammatory properties further contribute to its value in the pursuit of novel therapeutic agents.

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  • (E)-1-(3,6-dihydroxy-2,4-dimethoxy-phenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

    Cas No: 93993-77-2

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  • 93993-77-2 Structure

  • Basic information

    1. Product Name: (2E)-1-(3,6-dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one
    2. Synonyms: 1-(3,6-Dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)-2-propen-1-one; 3',6'-Dihydroxy-2',4,4'-trimethoxy-chalcone
    3. CAS NO:93993-77-2
    4. Molecular Formula: C18H18O6
    5. Molecular Weight: 330.3319
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93993-77-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 583°C at 760 mmHg
    3. Flash Point: 213.3°C
    4. Appearance: N/A
    5. Density: 1.276g/cm3
    6. Vapor Pressure: 3.43E-14mmHg at 25°C
    7. Refractive Index: 1.62
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (2E)-1-(3,6-dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2E)-1-(3,6-dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one(93993-77-2)
    12. EPA Substance Registry System: (2E)-1-(3,6-dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one(93993-77-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93993-77-2(Hazardous Substances Data)

93993-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93993-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,9 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93993-77:
(7*9)+(6*3)+(5*9)+(4*9)+(3*3)+(2*7)+(1*7)=192
192 % 10 = 2
So 93993-77-2 is a valid CAS Registry Number.

93993-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-(3,6-dihydroxy-2,4-dimethoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3'.6'-dihydroxy-4.2'.4'-trimethoxy-trans-chalcone

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:93993-77-2 SDS

93993-77-2Relevant articles and documents

A practical synthesis of the flavone, scutellarein

Wang, Qian,Liao, Xia-Li,Xiang, Cheng,Yang, Jian

, p. 157 - 159 (2017/03/27)

A practical and economical five-step synthesis of the flavone scutellarein has been achieved in 60% overall yield using the available and cheap 2,6-dimethoxy-1,4-benzoquinone as starting material. The reaction sequence involved reduction to the corresponding quinol, Friedel-Crafts acetylation, Claisen-Schmidt condensation with p-methoxybenzaldehyde, cyclisation and demethylation. The procedure is operationally simple and amenable to scale-up synthesis.

Regioselective hydroxylation of 2-hydroxychalcones by dimethyldioxirane towards polymethoxylated flavonoids

Chu, Han-Wei,Wu, Huan-Ting,Lee, Yean-Jang

, p. 2647 - 2655 (2007/10/03)

The flavone nucleus is part of a large number of natural products and medicinal compounds. In this presentation the novel regioselective hydroxylation of hydroxyarenes with DMD is described. The results showed further that flavonoids with 5-hydroxy group were selectively oxyfunctionalized at the para-position C8 carbon atom by DMD. Finally, according to this methodology, the naturally occurring isosinensetin, tangeretin, sinensetin, nobiletin, natsudaidain, gardenin B, 3,3′,4′,5,6,7,8- heptamethoxyflavone, quercetin and its derivatives were synthesized.

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