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83217-89-4

1β-Hydroxy-β-eudesMol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83217-89-4 Structure

  • Basic information

    1. Product Name: 1β-Hydroxy-β-eudesMol
    2. Synonyms: 1β-Hydroxy-β-eudesMol;(2R,4aR,5R,8aS)-Decahydro-5-hydroxy-alpha,alpha,4a-trimethyl-8-methylene-2-naphthalenemethanol;1beta-Hydroxy-beta-eudesmol
    3. CAS NO:83217-89-4
    4. Molecular Formula: C15H26O2
    5. Molecular Weight: 238.36574
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83217-89-4.mol

  • Chemical Properties

    1. Melting Point: 152℃
    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: 1β-Hydroxy-β-eudesMol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1β-Hydroxy-β-eudesMol(83217-89-4)
    11. EPA Substance Registry System: 1β-Hydroxy-β-eudesMol(83217-89-4)

  • 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: 83217-89-4(Hazardous Substances Data)

83217-89-4 Usage

General Description

1β-Hydroxy-β-eudesmol is a naturally occurring sesquiterpene alcohol found in essential oils of various aromatic plants. It is used in traditional medicine for its anti-inflammatory, antimicrobial, and antioxidant properties. Studies have shown that 1β-Hydroxy-β-eudesmol has potential in treating various diseases, including cancer, inflammatory diseases, and neurological disorders. It acts on multiple signaling pathways within the cells, leading to its diverse biological activities. Additionally, 1β-Hydroxy-β-eudesmol has demonstrated promising results as a potential therapeutic agent for treating drug-resistant bacterial infections due to its antimicrobial properties. Overall, 1β-Hydroxy-β-eudesmol is a compound with significant potential for pharmaceutical and therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 83217-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,2,1 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83217-89:
(7*8)+(6*3)+(5*2)+(4*1)+(3*7)+(2*8)+(1*9)=134
134 % 10 = 4
So 83217-89-4 is a valid CAS Registry Number.

83217-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,4aS,6R,8aR)-6-(2-hydroxypropan-2-yl)-8a-methyl-4-methylenedecahydronaphthalen-1-ol

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:83217-89-4 SDS

83217-89-4Downstream Products

83217-89-4Relevant articles and documents

SESQUITERPENES FROM LEAVES OF CRYPTOMERIA JAPONICA

Su, Wen-Chiung,Fang, Jim-Min,Cheng, Yu-Shia

, p. 603 - 608 (2007/10/02)

Twenty-seven sesquiterpenes were isolated from leaves of Cryptomeria japonica.The new compounds included elem-1-en-4,11-diol, 11-acetoxyeudesman-4α-ol, eudesmane-5α,11-diol, 3-eudesmene-1β,11-diol, 1β-acetoxy-3-eudesmen-11-ol, 4-eudesmene-1β,11-diol, 1β-acetoxy-4-eudesmen-11-ol, 7-epi-4-eudesmene-1β,11-diol, 1β-acetoxy-4(15)eudesmen-11-ol.Their structures were determined by chemical and spectral methods. - Key words: Cryptomeria japonica; Taxodiaceae; leaves; sesquiterpenes.

Total Synthesis of (+)-Balanitol and of (+)-Selin-4-(15)-ene-1β,11-diol

Anglea, Timothy A.,Pinder, A. Reginald

, p. 5537 - 5544 (2007/10/02)

(+)-Balanitol (1) and (+)-selin-4-(15)-ene-1β,11-diol (2), two recently isolated naturally occurring eudesmanoid bicyclic sesquiterpene alcohols, have been synthesized stereoselectively by a route involving a photocycloaddition of a cyclobutene and

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