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  • 1585-68-8 Structure
  • Basic information

    1. Product Name: Catalpalactone
    2. Synonyms: Catalpalactone
    3. CAS NO:1585-68-8
    4. Molecular Formula: C15H14O4
    5. Molecular Weight: 258.26926
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1585-68-8.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 467.1°C at 760 mmHg
    3. Flash Point: 245.2°C
    4. Appearance: /
    5. Density: 1.269g/cm3
    6. Vapor Pressure: 6.69E-09mmHg at 25°C
    7. Refractive Index: 1.575
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Catalpalactone(CAS DataBase Reference)
    11. NIST Chemistry Reference: Catalpalactone(1585-68-8)
    12. EPA Substance Registry System: Catalpalactone(1585-68-8)
  • 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: 1585-68-8(Hazardous Substances Data)

1585-68-8 Usage

Description

Catalpalactone, also known as 5-O-p-coumaroylcatalpol, is a natural product chemical compound derived from catalpa trees, particularly found in the leaves and root bark. It is an iridoid glycoside, a class of compounds known for their diverse biological activities. Catalpalactone has been studied for its potential anti-inflammatory, anti-tumor, and anti-oxidant properties, as well as its ability to induce apoptosis in cancer cells. Additionally, it has shown promise as an antiviral agent, specifically against herpes simplex virus type 1 (HSV-1). These diverse biological activities make catalpalactone a compound of interest for further research and potential therapeutic applications.

Uses

Used in Pharmaceutical Industry:
Catalpalactone is used as a potential anti-inflammatory agent for its ability to reduce inflammation, which can be beneficial in treating various inflammatory conditions.
Catalpalactone is used as a potential anti-tumor agent for its ability to induce apoptosis in cancer cells, making it a candidate for cancer treatment research.
Catalpalactone is used as a potential anti-oxidant agent for its ability to neutralize harmful free radicals, which can protect cells from oxidative damage and contribute to overall health.
Used in Antiviral Applications:
Catalpalactone is used as a potential antiviral agent, specifically against herpes simplex virus type 1 (HSV-1), for its ability to inhibit viral replication and reduce the severity of infections.
Used in Cancer Research:
Catalpalactone is used as a potential anti-cancer agent for its ability to induce apoptosis in cancer cells, making it a promising candidate for further research into cancer treatment strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 1585-68-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1585-68:
(6*1)+(5*5)+(4*8)+(3*5)+(2*6)+(1*8)=98
98 % 10 = 8
So 1585-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O4/c1-15(2)8-7-11(14(17)19-15)12-9-5-3-4-6-10(9)13(16)18-12/h3-7,12H,8H2,1-2H3

1585-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,2-dimethyl-6-oxo-3H-pyran-5-yl)-3H-2-benzofuran-1-one

1.2 Other means of identification

Product number -
Other names Catalpalactone

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:1585-68-8 SDS

1585-68-8Downstream Products

1585-68-8Relevant articles and documents

New Synthesis of Catalpalactone

Chordia, Mahendra D.,Narasimhan, Nurani S.

, p. 371 - 376 (2007/10/02)

Various alkylidenephthalides (E- and Z-5, 6 and 7) were prepared by Wittig reaction of phosphoranes 4a, 4b and 4c respectively with phthalic anhydride.The products were then lactonised, using chloro(trimethyl)silane and sodium iodide, to the corresponding

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