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(E)-4-(2-methoxyimino-2-[2-(o-tolyloxymethyl)phenyl]acetamido)butanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1007364-32-0 Structure
  • Basic information

    1. Product Name: (E)-4-(2-methoxyimino-2-[2-(o-tolyloxymethyl)phenyl]acetamido)butanoic acid
    2. Synonyms: (E)-4-(2-methoxyimino-2-[2-(o-tolyloxymethyl)phenyl]acetamido)butanoic acid
    3. CAS NO:1007364-32-0
    4. Molecular Formula:
    5. Molecular Weight: 384.432
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1007364-32-0.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: (E)-4-(2-methoxyimino-2-[2-(o-tolyloxymethyl)phenyl]acetamido)butanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-(2-methoxyimino-2-[2-(o-tolyloxymethyl)phenyl]acetamido)butanoic acid(1007364-32-0)
    11. EPA Substance Registry System: (E)-4-(2-methoxyimino-2-[2-(o-tolyloxymethyl)phenyl]acetamido)butanoic acid(1007364-32-0)
  • 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: 1007364-32-0(Hazardous Substances Data)

1007364-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1007364-32-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,3,6 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1007364-32:
(9*1)+(8*0)+(7*0)+(6*7)+(5*3)+(4*6)+(3*4)+(2*3)+(1*2)=110
110 % 10 = 0
So 1007364-32-0 is a valid CAS Registry Number.

1007364-32-0Downstream Products

1007364-32-0Relevant articles and documents

Hapten synthesis and monoclonal antibody-based immunoassay development for the detection of the fungicide kresoxim-methyl

Mercader, Josep V.,Suarez-Pantaleon, Celia,Agullo, Consuelo,Abad-Somovilla, Antonio,Abad-Fuentes, Antonio

experimental part, p. 1545 - 1552 (2009/07/18)

Strobilurin fungicides have been increasingly used for fungus pest control since they were introduced in 1996. For pesticide residue detection, immunoassays constitute nowadays a valuable approach. This paper describes the synthesis of functionalized haptens of kresoxim-methyl, the production of monoclonal antibodies, and the development of enzyme-linked immunosorbent assays. On the one hand, a two-step conjugate-coated immunoassay was optimized using extended or short incubation times, with limits of detection of 0.4 ng/mL for the extended assay and 0.3 ng/mL for the rapid assay. On the other hand, an immunoassay was optimized following a procedure consisting of just one incubation step. This one-step assay had a limit of detection of 0.4 ng/mL. All of these assays showed a similar performance, with sensitivities well below common maximum residue limits for this pesticide (50 μg/kg) and lower than the detection limits of the usual chromatographic detection methods.

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