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503559-74-8

4-(2-benzyloxy-4-fluoro-phenyl)-2,6-diisopropyl-5-vinyl-nicotinic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 4-(2-benzyloxy-4-fluoro-phenyl)-2,6-diisopropyl-5-vinyl-nicotinic acid methyl ester

    Cas No: 503559-74-8

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  • 503559-74-8 Structure

  • Basic information

    1. Product Name: 4-(2-benzyloxy-4-fluoro-phenyl)-2,6-diisopropyl-5-vinyl-nicotinic acid methyl ester
    2. Synonyms:
    3. CAS NO:503559-74-8
    4. Molecular Formula:
    5. Molecular Weight: 447.55
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 503559-74-8.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: 4-(2-benzyloxy-4-fluoro-phenyl)-2,6-diisopropyl-5-vinyl-nicotinic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(2-benzyloxy-4-fluoro-phenyl)-2,6-diisopropyl-5-vinyl-nicotinic acid methyl ester(503559-74-8)
    11. EPA Substance Registry System: 4-(2-benzyloxy-4-fluoro-phenyl)-2,6-diisopropyl-5-vinyl-nicotinic acid methyl ester(503559-74-8)

  • 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: 503559-74-8(Hazardous Substances Data)

503559-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 503559-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,5,5 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 503559-74:
(8*5)+(7*0)+(6*3)+(5*5)+(4*5)+(3*9)+(2*7)+(1*4)=148
148 % 10 = 8
So 503559-74-8 is a valid CAS Registry Number.

503559-74-8Relevant articles and documents

Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists

Ladouceur, Gaetan H.,Cook, James H.,Hertzog, Donald L.,Jones,Hundertmark, Thomas,Korpusik, Mary,Lease, Timothy G.,Livingston, James N.,MacDougall, Margit L.,Osterhout, Martin H.,Phelan, Kathleen,Romero, Romulo H.,Schoen, William R.,Shao, Chunning,Smith, Roger A.

, p. 3421 - 3424 (2007/10/03)

Optimized substituent patterns in 4-aryl-pyridine glucagon receptor antagonists were merged to produce highly potent derivatives containing both a 3-[(1R)-hydroxyethyl] and a 2′-hydroxy group. Due to restricted rotation of the phenyl-pyridine bond, these analogues exist as four isomers. A diastereoselective methylcopper reaction was developed to facilitate the synthesis, and single isomers were isolated with activities in the range IC50=10-25 nM.

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