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4',9,9'-Trihydroxy-3'-methoxy-3,7'-epoxy-4,8'-oxyneolignan is a naturally occurring compound that belongs to the neolignan class of chemicals. It is characterized by its unique chemical structure, which includes three hydroxyl groups, a methoxy group, and an epoxy ring. 4',9,9'-Trihydroxy-3'-methoxy-
3,7'-epoxy-4,8'-oxyneolignan is found in various plant species and is known for its antioxidant and anti-inflammatory properties. Its potential therapeutic applications have been studied, with research indicating that it may protect against oxidative stress, reduce inflammation, and potentially inhibit the growth of cancer cells. Furthermore, 4',9,9'-Trihydroxy-3'-methoxy-3,7'-epoxy-4,8'-oxyneolignan has shown promise in neuroprotective and cardiovascular benefits, making it a valuable target for further investigation and potential drug development.

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  • 144881-21-0 Structure
  • Basic information

    1. Product Name: 4',9,9'-Trihydroxy-3'-methoxy- 3,7'-epoxy-4,8'-oxyneolignan
    2. Synonyms: 4',9,9'-Trihydroxy-3'-methoxy- 3,7'-epoxy-4,8'-oxyneolignan;(2S,3S)-2,3-Dihydro-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-1,4-benzodioxin-6-propanol
    3. CAS NO:144881-21-0
    4. Molecular Formula: C19H22O6
    5. Molecular Weight: 346.37438
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144881-21-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4',9,9'-Trihydroxy-3'-methoxy- 3,7'-epoxy-4,8'-oxyneolignan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4',9,9'-Trihydroxy-3'-methoxy- 3,7'-epoxy-4,8'-oxyneolignan(144881-21-0)
    11. EPA Substance Registry System: 4',9,9'-Trihydroxy-3'-methoxy- 3,7'-epoxy-4,8'-oxyneolignan(144881-21-0)
  • 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: 144881-21-0(Hazardous Substances Data)

144881-21-0 Usage

Uses

Used in Antioxidant Applications:
4',9,9'-Trihydroxy-3'-methoxy-3,7'-epoxy-4,8'-oxyneolignan is used as an antioxidant agent for its ability to protect against oxidative stress. Its antioxidant properties make it a potential candidate for use in various health and wellness applications, as well as in the development of pharmaceuticals aimed at reducing oxidative damage in the body.
Used in Anti-Inflammatory Applications:
In the field of anti-inflammatory applications, 4',9,9'-Trihydroxy-3'-methoxy-3,7'-epoxy-4,8'-oxyneolignan is used to reduce inflammation. Its anti-inflammatory properties suggest that it could be beneficial in treating conditions characterized by excessive inflammation, such as arthritis or other inflammatory disorders.
Used in Cancer Therapy:
4',9,9'-Trihydroxy-3'-methoxy-3,7'-epoxy-4,8'-oxyneolignan is used as a potential cancer therapy agent due to its ability to inhibit the growth of cancer cells. Its potential role in cancer treatment is currently under investigation, with research exploring its effects on various types of cancer and its potential synergistic effects when combined with conventional cancer therapies.
Used in Neuroprotective Applications:
In the field of neuroprotection, 4',9,9'-Trihydroxy-3'-methoxy-3,7'-epoxy-4,8'-oxyneolignan is used for its potential neuroprotective benefits. Research has shown that this compound may help protect neurons from damage, making it a promising candidate for the development of treatments for neurodegenerative diseases such as Alzheimer's or Parkinson's.
Used in Cardiovascular Applications:
4',9,9'-Trihydroxy-3'-methoxy-3,7'-epoxy-4,8'-oxyneolignan is used in cardiovascular applications for its potential cardiovascular benefits. Its effects on the cardiovascular system are currently being studied, with the aim of developing new treatments for heart disease and other related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 144881-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,8 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 144881-21:
(8*1)+(7*4)+(6*4)+(5*8)+(4*8)+(3*1)+(2*2)+(1*1)=140
140 % 10 = 0
So 144881-21-0 is a valid CAS Registry Number.

144881-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(2S,3S)-3-(Hydroxymethyl)-7-(3-hydroxypropyl)-2,3-dihydro-1,4- benzodioxin-2-yl]-2-methoxyphenol

1.2 Other means of identification

Product number -
Other names Arbo 4

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:144881-21-0 SDS

144881-21-0Downstream Products

144881-21-0Relevant articles and documents

New neolignan and phenylpropanoid glycosides in Juniperus communis var. depressa

Nakanishi, Tsutomu,Iida, Naoki,Inatomi, Yuka,Murata, Hiroko,Inada, Akira,Murata, Jin,Lang, Frank A.,Iinuma, Munekazu,Tanaka, Toshiyuki

, p. 2573 - 2580 (2007/10/03)

Two new neolignan glucosides (junipercomnosides C and D) and two new phenypropanoid glycosides (junipercomnosides E and F) were isolated from aerial parts of Juniperus communia var. depressa along with seven known phenylpropanoid glycosides. The structures of the isolated compounds were determined by spectral analysis, in particular by the detailed analysis of 2D NMR and CD spectra.

First asymmetric synthesis of chiral 1,4-benzodioxane lignans

Gu,Jing,Pan,Chan,Yang

, p. 6079 - 6082 (2007/10/03)

An asymmetric and regioselective total synthesis approach to 1,4-benzodioxane lignans was reported in which (2R,3R)- and (2S,3S)-3-(4-hydroxy-3-methoxyphenyl)-2-hydroxymethyl-1,4-benzodi oxan-6-carbaldehyde were synthesized firstly. A natural 1,4-benzodioxane neolignan was synthesized firstly by the synthesis approach. (C) 2000 Elsevier Science Ltd.

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