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Methyl demethoxycarbonylchafruticosinate is a naturally occurring chemical compound found in various plant species, particularly in the Chrysanthemum genus. It is classified as a pyrethrin, a group of organic compounds known for their insecticidal properties. Methyl demethoxycarbonylchafruticosinate is recognized for its ability to effectively deter and control a wide range of pests, making it a valuable component in various applications.

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  • 80151-89-9 Structure
  • Basic information

    1. Product Name: Methyl demethoxycarbonylchafruticosinate
    2. Synonyms: Methyl demethoxycarbonylchafruticosinate;Methyl deMethoxycarbonylchanofruticosinate;Des-N-(methoxycarbonyl)chanofruticosinic acid methyl ester;Methyl N-(decarbomethoxy)chanofruticosinate
    3. CAS NO:80151-89-9
    4. Molecular Formula: C21H24N2O3
    5. Molecular Weight: 352.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80151-89-9.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: Methyl demethoxycarbonylchafruticosinate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl demethoxycarbonylchafruticosinate(80151-89-9)
    11. EPA Substance Registry System: Methyl demethoxycarbonylchafruticosinate(80151-89-9)
  • 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: 80151-89-9(Hazardous Substances Data)

80151-89-9 Usage

Uses

Used in Pest Control Industry:
Methyl demethoxycarbonylchafruticosinate is used as an active ingredient in insect repellents and pesticides for its potent insecticidal properties. It is effective in deterring and controlling a broad spectrum of pests, including mosquitoes, flies, and cockroaches, which makes it a crucial component in protecting crops and maintaining hygiene in various settings.
Used in Environmentally Friendly Practices:
Recognized as a relatively safe and environmentally friendly alternative to synthetic insecticides, Methyl demethoxycarbonylchafruticosinate is used in organic and sustainable farming practices. Its use aligns with the goals of reducing the environmental impact of pest control methods and promoting ecological balance.
Used in Public Health Initiatives:
Given its effectiveness against disease-carrying insects such as mosquitoes, Methyl demethoxycarbonylchafruticosinate is utilized in public health initiatives aimed at reducing the spread of vector-borne diseases. Its incorporation into insect repellents and other pest control measures contributes to improving community health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 80151-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,5 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80151-89:
(7*8)+(6*0)+(5*1)+(4*5)+(3*1)+(2*8)+(1*9)=109
109 % 10 = 9
So 80151-89-9 is a valid CAS Registry Number.

80151-89-9SDS

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 Methyl demethoxycarbonylchanofruticosinate

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:80151-89-9 SDS

80151-89-9Downstream Products

80151-89-9Relevant articles and documents

Total synthesis of the indole alkaloid (±)- and (+)-methyl N-decarbomethoxychanofruticosinate

Wei, Yi,Zhao, Duo,Ma, Dawei

, p. 12988 - 12991 (2013)

All caged up: The first total synthesis of N- decarbomethoxychanofruticosinate (see figure) is achieved by using a SmI 2-mediated intramolecular Reformatsky-like reaction to create the seven-membered ring, and an intramolecular oxidative coupling to install the caged and strained ring system. Copyright

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