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CAS

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30766-27-9

methyl 5-nitronicotinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30766-27-9 Structure

  • Basic information

    1. Product Name: methyl 5-nitronicotinate
    2. Synonyms: methyl 5-nitronicotinate
    3. CAS NO:30766-27-9
    4. Molecular Formula: C7H6N2O4
    5. Molecular Weight: 182.13354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30766-27-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 287.3±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.375±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -0.84±0.20(Predicted)
    10. CAS DataBase Reference: methyl 5-nitronicotinate(CAS DataBase Reference)
    11. NIST Chemistry Reference: methyl 5-nitronicotinate(30766-27-9)
    12. EPA Substance Registry System: methyl 5-nitronicotinate(30766-27-9)

  • 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: 30766-27-9(Hazardous Substances Data)

30766-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30766-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,6 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30766-27:
(7*3)+(6*0)+(5*7)+(4*6)+(3*6)+(2*2)+(1*7)=109
109 % 10 = 9
So 30766-27-9 is a valid CAS Registry Number.

30766-27-9Downstream Products

30766-27-9Relevant articles and documents

Reactions of 3-R-5-nitropyridines with nucleophiles: Nucleophilic substitution vs conjugate addition

Bastrakov, Maxim A.,Nikol'skiy, Vladislav V.,Starosotnikov, Alexey M.,Fedyanin, Ivan V.,Shevelev, Svyatoslav A.,Knyazev, Daniil A.

, (2019/11/11)

A number of 3-R-5-nitropyridines were synthesized and their reactions with various types of nucleophiles were investigated. The reaction outcome depends on the nature of a nucleophile: in case of anionic O-, N- and S-nucleophiles the previously unreported substitution of non-activated nitro group occurred while carbon nucleophiles underwent dearomatization of the pyridine ring with the formation of products of 1,2- and 1,4-addition.

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