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116499-73-1

9α,13α-Epidioxyabiet-8(14)-en-18-oic acid is a naturally occurring diterpene compound characterized by its unique epoxy ring structure. It is found in certain plants and has demonstrated potential anti-inflammatory and cytotoxic activities, making it a promising candidate for medical and pharmaceutical applications.

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  • 116499-73-1 Structure

  • Basic information

    1. Product Name: 9α,13α-Epidioxyabiet-8(14)-en-18-oic acid
    2. Synonyms: 9α,13α-Epidioxyabiet-8(14)-en-18-oic acid;9alpha,13alpha-Epidioxyabiet-8(14)-en-18-oic acid
    3. CAS NO:116499-73-1
    4. Molecular Formula: C20H30O4
    5. Molecular Weight: 334.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116499-73-1.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: 9α,13α-Epidioxyabiet-8(14)-en-18-oic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9α,13α-Epidioxyabiet-8(14)-en-18-oic acid(116499-73-1)
    11. EPA Substance Registry System: 9α,13α-Epidioxyabiet-8(14)-en-18-oic acid(116499-73-1)

  • 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: 116499-73-1(Hazardous Substances Data)

116499-73-1 Usage

Uses

Used in Pharmaceutical Industry:
9α,13α-Epidioxyabiet-8(14)-en-18-oic acid is used as a potential therapeutic agent for treating various inflammatory conditions due to its anti-inflammatory properties. Its ability to modulate inflammatory responses makes it a valuable compound for further research and development in the treatment of chronic inflammatory diseases.
Used in Anticancer Applications:
9α,13α-Epidioxyabiet-8(14)-en-18-oic acid is used as a potential anticancer agent, exhibiting cytotoxic effects against cancer cells. Its unique chemical structure and biological activities make it an intriguing target for further research in the development of novel cancer therapies.
Used in Drug Development:
9α,13α-Epidioxyabiet-8(14)-en-18-oic acid is used as a target for drug development due to its potential medical applications. Its unique properties and biological activities make it a valuable compound for the discovery of new drugs with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 116499-73-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,9 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116499-73:
(8*1)+(7*1)+(6*6)+(5*4)+(4*9)+(3*9)+(2*7)+(1*3)=151
151 % 10 = 1
So 116499-73-1 is a valid CAS Registry Number.

116499-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (1R,4aR,5R,8R,8aR)-8-(benzoyloxy)-5-(3-formyl-3-buten-1-yl )-4a-methyl-6-methylenedecahydro-1-naphthalenecarboxylate

1.2 Other means of identification

Product number -
Other names -

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:116499-73-1 SDS

116499-73-1Downstream Products

116499-73-1Relevant articles and documents

Abietane diterpenes from the cones of Cedrus atlantica

Barrero, Alejandro F.,Quílez Del Moral, José F.,Mar Herrador,Arteaga, Jesus F.,Akssira, Mohamed,Benharref, Ahmed,Dakir, Mohamed

, p. 105 - 111 (2005)

Five new abietanes, three of them isolated as the corresponding acetate derivatives, i.e., 9α,13α-epidioxiabiet-8(14)-en-18-ol, 7α,18-diacetoxy, 9β,13β-epidioxiabiet-8(14)-ene, 7α,18-diacetoxyabiet-8(14)-en-13β-ol, 7α,18-diacetoxy-13β- methoxyabiet-8(14)-ene, and 13β-hydroxyabiet-8(14)-en-7-one, were isolated from the neutral part of the hexane extract of the cones of Cedrus atlantica collected in Middle Atlas, Morocco. The structures of these compounds were established by spectroscopic techniques, including 2D NMR spectra, and in the case of 1, by chemical correlation. The cytotoxicity of these abietane diterpenoids was tested against five cell lines.

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