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CAS

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306950-79-8

ethyl 2-[N-(mesitylacetyl)-N-(methoxy)]amino-2-methylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 306950-79-8 Structure

  • Basic information

    1. Product Name: ethyl 2-[N-(mesitylacetyl)-N-(methoxy)]amino-2-methylpropanoate
    2. Synonyms: ethyl 2-[N-(mesitylacetyl)-N-(methoxy)]amino-2-methylpropanoate
    3. CAS NO:306950-79-8
    4. Molecular Formula:
    5. Molecular Weight: 321.417
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 306950-79-8.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: ethyl 2-[N-(mesitylacetyl)-N-(methoxy)]amino-2-methylpropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-[N-(mesitylacetyl)-N-(methoxy)]amino-2-methylpropanoate(306950-79-8)
    11. EPA Substance Registry System: ethyl 2-[N-(mesitylacetyl)-N-(methoxy)]amino-2-methylpropanoate(306950-79-8)

  • 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: 306950-79-8(Hazardous Substances Data)

306950-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 306950-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,9,5 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 306950-79:
(8*3)+(7*0)+(6*6)+(5*9)+(4*5)+(3*0)+(2*7)+(1*9)=148
148 % 10 = 8
So 306950-79-8 is a valid CAS Registry Number.

306950-79-8Downstream Products

306950-79-8Relevant articles and documents

Synthesis of N-oxydihydropyrrole derivatives

Ito, Mitsuru,Okui, Hideshi,Nakagawa, Harumi,Mio, Shigeru,Iwasaki, Toshiaki,Iwabuchi, Jun

, p. 881 - 894 (2007/10/03)

N-Oxydihydropyrrole derivatives were synthesized through an intramolecular Claisen condensation reaction. The N-acylation of hindered hydroxylamines played a key role in providing the useful intermediates, which could be converted to a variety of N-oxydihydropyrrole derivatives.

Synthesis and Insecticidal Activity of N-Oxydihydropyrroles: 4-Hydroxy-3-mesityl-5,5-dimethyl Derivatives with Various Substituents at the 1-Position

Iro, Mitsuru,Okui, Hideshi,Nakagawa, Harumi,Mio, Shigeru,Kinoshita, Ayako,Obayashi, Takashi,Miura, Takako,Nagai, Junko,Yokoi, Shinji,Ichinose, Reiji,Tanaka, Keiji,et al.

, p. 2406 - 2414 (2007/10/03)

A new series of N-oxydihydropyrrole derivatives was synthesized and evaluated for insecticidal activity against Nilaparvata lugens and Myzus persicae. Various substituents were introduced to the 1-position of the dihydropyrrole ring, and the derivatives obtained exhibited systemic and/or contact insecticidal activity. The structure-activity relationship revealed that small alkyoxy and alkoxyalkoxy groups were more favorable than alkylcarbonyloxy, alkoxycarbonyloxy, or sulfonyloxy groups as substituents at the 1-position.

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