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156722-99-5

2-Propenoic acid, 5-chloro-2-(2,4-dichlorophenoxy)phenyl ester, also known as cloxifenfurum, is a synthetic chemical compound belonging to the class of phenoxy herbicides. It is primarily used in agriculture to control broadleaf weeds and grasses in various crops, including cereals, sugar beets, and potatoes. The compound is characterized by its molecular structure, which features a 5-chloro-2-(2,4-dichlorophenoxy)phenyl group esterified to the 2-propenoic acid moiety. Cloxifenfurum works by inhibiting the growth of weeds by disrupting their cell membrane function and photosynthesis process. Due to its selective nature, it is effective in controlling weeds without causing significant harm to the desired crops. However, it is essential to follow proper application guidelines to minimize potential risks to non-target plants, soil, and aquatic ecosystems.

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  • 156722-99-5 Structure

  • Basic information

    1. Product Name: 2-Propenoic acid, 5-chloro-2-(2,4-dichlorophenoxy)phenyl ester
    2. Synonyms:
    3. CAS NO:156722-99-5
    4. Molecular Formula: C15H9Cl3O3
    5. Molecular Weight: 343.594
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156722-99-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Propenoic acid, 5-chloro-2-(2,4-dichlorophenoxy)phenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propenoic acid, 5-chloro-2-(2,4-dichlorophenoxy)phenyl ester(156722-99-5)
    11. EPA Substance Registry System: 2-Propenoic acid, 5-chloro-2-(2,4-dichlorophenoxy)phenyl ester(156722-99-5)

  • 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: 156722-99-5(Hazardous Substances Data)

156722-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156722-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 156722-99:
(8*1)+(7*5)+(6*6)+(5*7)+(4*2)+(3*2)+(2*9)+(1*9)=155
155 % 10 = 5
So 156722-99-5 is a valid CAS Registry Number.

156722-99-5SDS

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 [5-chloro-2-(2,4-dichlorophenoxy)phenyl] prop-2-enoate

1.2 Other means of identification

Product number -
Other names 5-chloro-2-(2,4-dichlorophenoxy)phenyl acrylate

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:156722-99-5 SDS

156722-99-5Downstream Products

156722-99-5Relevant articles and documents

ANTIMICROBIAL COMPOSITIONS

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Page/Page column 14, (2010/04/28)

Provided are antimicrobial compositions including at least one biocide covalently bound to a polyurethane. The biocide moiety may comprise triclosan, a triclosan derivative, or a quaternary ammonium salt. Further provided are methods of reducing biofilm formation or microbial growth on a surface, the method including applying to the surface an antimicrobial composition including at least one biocide covalently attached to a polyurethane.

Polymeric delivery and release systems for oral care actives

-

, (2008/06/13)

A polymer useful in oral care compositions which has a reactive group covalently bonded to a bactericide, flavorant and/or essential oil compound, said bond being hydrolyzable in aqueous solution to slowly release said compound into said composition.

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