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METHYL 6-(BENZYLAMINO)-5-CYANO-2-METHYLNICOTINATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 303146-89-6 Structure
  • Basic information

    1. Product Name: METHYL 6-(BENZYLAMINO)-5-CYANO-2-METHYLNICOTINATE
    2. Synonyms: METHYL 6-(BENZYLAMINO)-5-CYANO-2-METHYLNICOTINATE;methyl 6-(benzylamino)-5-cyano-2-methylpyridine-3-carboxylate
    3. CAS NO:303146-89-6
    4. Molecular Formula: C16H15N3O2
    5. Molecular Weight: 281.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 303146-89-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 446.0±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.23±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 1.87±0.10(Predicted)
    10. CAS DataBase Reference: METHYL 6-(BENZYLAMINO)-5-CYANO-2-METHYLNICOTINATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: METHYL 6-(BENZYLAMINO)-5-CYANO-2-METHYLNICOTINATE(303146-89-6)
    12. EPA Substance Registry System: METHYL 6-(BENZYLAMINO)-5-CYANO-2-METHYLNICOTINATE(303146-89-6)
  • 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: 303146-89-6(Hazardous Substances Data)

303146-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 303146-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,1,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 303146-89:
(8*3)+(7*0)+(6*3)+(5*1)+(4*4)+(3*6)+(2*8)+(1*9)=106
106 % 10 = 6
So 303146-89-6 is a valid CAS Registry Number.

303146-89-6Downstream Products

303146-89-6Relevant articles and documents

Synthesis, inhibitory activity of cholinesterases, and neuroprotective profile of novel 1,8-naphthyridine derivatives

De Los Ríos, Cristóbal,Egea, Javier,Marco-Contelles, José,León, Rafael,Samadi, Abdelouahid,Iriepa, Isabel,Moraleda, Ignacio,Gálvez, Enrique,García, Antonio G.,López, Manuela G.,Villarroya, Mercedes,Romero, Alejandro

experimental part, p. 5129 - 5143 (2010/09/14)

1,8-Naphthyridine derivatives related to 17 (ITH4012), a neuroprotective compound reported by our research group, have been synthesized. In general, they have shown better inhibition of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) than mo

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