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Ipomeamarone, a naturally occurring naphthoquinone compound, is found in the seeds of the Ipomoea carnea plant, commonly known as white morning glory. It has demonstrated potential anticancer and cytotoxic properties, making it a promising candidate for the development of new anticancer drugs.

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  • 2-Pentanone, 4-methyl-1- (2,3,4,5-tetrahydro-5-methyl[2, 3-bifuran]-5-yl)-

    Cas No: 20007-82-3

  • USD $ 1.9-2.9 / Gram

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  • 20007-82-3 Structure
  • Basic information

    1. Product Name: ipomeamarone
    2. Synonyms: ipomeamarone;4-Methyl-1-(2,3,4,5-tetrahydro-5-methyl-2,3'-bifuran-5-yl)-2-pentanone
    3. CAS NO:20007-82-3
    4. Molecular Formula: C15H22O3
    5. Molecular Weight: 250.33338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20007-82-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 343.6°Cat760mmHg
    3. Flash Point: 161.6°C
    4. Appearance: /
    5. Density: 1.016g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ipomeamarone(CAS DataBase Reference)
    10. NIST Chemistry Reference: ipomeamarone(20007-82-3)
    11. EPA Substance Registry System: ipomeamarone(20007-82-3)
  • 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: 20007-82-3(Hazardous Substances Data)

20007-82-3 Usage

Uses

Used in Pharmaceutical Industry:
Ipomeamarone is used as a potential anticancer agent for its ability to induce cell death in various cancer cell lines. Its mechanism of action and potential therapeutic applications are still under investigation, with further research needed to fully understand its capabilities and optimize its use in cancer treatment.
Used in Cancer Research:
In the field of cancer research, ipomeamarone is utilized as a subject of study to explore its potential as a novel anticancer drug. Its cytotoxic properties and effects on cancer cell lines are being investigated to determine its efficacy and possible synergistic effects with existing treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 20007-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,0 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20007-82:
(7*2)+(6*0)+(5*0)+(4*0)+(3*7)+(2*8)+(1*2)=53
53 % 10 = 3
So 20007-82-3 is a valid CAS Registry Number.

20007-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name BOHLMANN 176

1.2 Other means of identification

Product number -
Other names trans-4-methyl-1-(2,3,4,5-tetrahydro-5-methyl<2,3'-bifuran>-5-yl)-2-pentanone

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:20007-82-3 SDS

20007-82-3Downstream Products

20007-82-3Relevant articles and documents

Formal Total Synthesis of Ipomeamarone via the Dihydrofuran Annulation

Hudlicky, Tomas,Lovelace, Thomas C.

, p. 1721 - 1732 (2007/10/02)

A formal synthesis of (2R-cis)-4-methyl-1-(2,3,4,5-tetrahydro)-5-methyl--2-pentanone, or ipomeamarone (1) was accomplished from 3-furaldehyde 5 and ethyl-2-bromocrotonate 4.The key step involved the formation of the dihydrofuran ring in 2 via a vinyloxirane rearrangement of 3 in the dihydrofuran annulation.Mechanistic duality of reactions of those tetrahydrofurans possessing acidic hydrogens adjacent to the ring is addressed.

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