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127234-68-8

1-BENZYL-3-(BENZYLOXY)-2-METHYL-4(1H)-PYRIDINONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127234-68-8 Structure

  • Basic information

    1. Product Name: 1-BENZYL-3-(BENZYLOXY)-2-METHYL-4(1H)-PYRIDINONE
    2. Synonyms: 1-BENZYL-3-(BENZYLOXY)-2-METHYL-4(1H)-PYRIDINONE;1-benzyl-3-(benzyloxy)-2-methyl-1,4-dihydropyridin-4-one
    3. CAS NO:127234-68-8
    4. Molecular Formula: C20H19NO2
    5. Molecular Weight: 305.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127234-68-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-BENZYL-3-(BENZYLOXY)-2-METHYL-4(1H)-PYRIDINONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-BENZYL-3-(BENZYLOXY)-2-METHYL-4(1H)-PYRIDINONE(127234-68-8)
    11. EPA Substance Registry System: 1-BENZYL-3-(BENZYLOXY)-2-METHYL-4(1H)-PYRIDINONE(127234-68-8)

  • 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: 127234-68-8(Hazardous Substances Data)

127234-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127234-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,2,3 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127234-68:
(8*1)+(7*2)+(6*7)+(5*2)+(4*3)+(3*4)+(2*6)+(1*8)=118
118 % 10 = 8
So 127234-68-8 is a valid CAS Registry Number.

127234-68-8Relevant articles and documents

Altering pyridinone N-substituents to optimise activity as potential prodrugs for Alzheimer's disease

Scott, Lauren E.,Page, Brent D. G.,Patrick, Brian O.,Orvig, Chris

, p. 6364 - 6367 (2008)

Selective design modifications of specifically substituted 3-hydroxy-4(1H)-pyridinones show possibly advantageous ring freedom while maintaining metal-binding ability and antioxidant capacity, moving toward an efficient potential treatment for Alzheimer's disease.

Synthesis, molecular modelling and biological studies of 3-hydroxy-pyrane-4-one and 3-hydroxy-pyridine-4-one derivatives as HIV-1 integrase inhibitors

Sirous, Hajar,Fassihi, Afshin,Brogi, Simone,Campiani, Giuseppe,Christ, Frauke,Debyser, Zeger,Gemma, Sandra,Butini, Stefania,Chemi, Giulia,Grillo, Alessandro,Zabihollahi, Rezvan,Aghasadeghi, Mohammad R.,Saghaie, Lotfollah,Memarian, Hamid R.

, p. 755 - 770 (2019/11/02)

Background: Despite the progress in the discovery of antiretroviral compounds for treating HIV-1 infection by targeting HIV integrase (IN), a promising and well-known drug target against HIV-1, there is a growing need to increase the armamentarium against

Monobactam hydrazide derivatives

-

, (2008/06/13)

Compounds having the formula I and pharmaceutically acceptable salts thereof which possess antibacterial activity. Rs is a substituted hydroxy pyridone of the formulae: II and III wherein Y1 is CH2X; COOR6; CONR7R8; OH; OCH2R9; CHF2; CHO; CH=N-OR10; CH=CH-R11; CN; CH=N-NHR12, and Y2 is hydrogen; COOH; CONH2; CN; CSNH2; COO lower alkyl; CONR7/R8

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