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3,5-Pyridinedicarboxylic acid, 4-(2-methoxyphenyl)-2,6-dimethyl-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3,5-Pyridinedicarboxylic acid, 4-(2-methoxyphenyl)-2,6-dimethyl-, diethyl ester

    Cas No: 115722-00-4

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  • 115722-00-4 Structure
  • Basic information

    1. Product Name: 3,5-Pyridinedicarboxylic acid, 4-(2-methoxyphenyl)-2,6-dimethyl-, diethyl ester
    2. Synonyms:
    3. CAS NO:115722-00-4
    4. Molecular Formula: C20H23NO5
    5. Molecular Weight: 357.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115722-00-4.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: 3,5-Pyridinedicarboxylic acid, 4-(2-methoxyphenyl)-2,6-dimethyl-, diethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-Pyridinedicarboxylic acid, 4-(2-methoxyphenyl)-2,6-dimethyl-, diethyl ester(115722-00-4)
    11. EPA Substance Registry System: 3,5-Pyridinedicarboxylic acid, 4-(2-methoxyphenyl)-2,6-dimethyl-, diethyl ester(115722-00-4)
  • 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: 115722-00-4(Hazardous Substances Data)

115722-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115722-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,2 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115722-00:
(8*1)+(7*1)+(6*5)+(5*7)+(4*2)+(3*2)+(2*0)+(1*0)=94
94 % 10 = 4
So 115722-00-4 is a valid CAS Registry Number.

115722-00-4Relevant articles and documents

TEMPO supported amine functionalized magnetic titania: a magnetically recyclable catalyst for the aerobic oxidative synthesis of heterocyclic compounds

Sharma, Sukanya,Choudhary, Anu,Sharma, Shally,Shamim, Tahira,Paul, Satya

, p. 83 - 94 (2021)

Abstract: The present protocol uncover a new strategy to synthesize highly efficient solid TEMPO based catalyst in which 4-oxo-TEMPO was covalently tethered to the surface of amine functionalized magnetic titania. The chemical nature and structure of the

Rapid and efficient oxidation of Hantzsch 1,4-dihydropyridines with sodium periodate catalyzed by manganese (III) Schiff base complexes

Nasr-Esfahani, Masoud,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Momeni, Ahmad Reza

, p. 2720 - 2724 (2006)

Rapid and efficient oxidation of Hantzsch 1,4-dihydropyridine with sodium periodate is reported. The Mn(III)-salophen/NaIO4 catalytic system converts 1,4-dihydropyridines to their corresponding pyridine derivatives at room temperature in a 1:1,

Aromatization of 1,4-dihydropyridines in the presence of toluenesulfonyl choloride/NaNO2/WET-SiO2 under microwave irradiation

Niknam, Khodabakhsh,Zolfigol, Mohammah Ali,Rabani, Farideh

, p. 183 - 186 (2006)

A combination of toluenesulfonyl chloride and sodium nitrite in the presence of wet SiO2 was used as an effective oxidizing agent for the aromatization of 1,4-dihydropyridines to the corresponding pyridine derivatives under microwave irradiatio

Tungstate sulfuric acid/ KMnO4 as a novel heterogeneous system for the rapid aromatization of hantzsch 1, 4-dihydropyridines under mild conditions

Karami, Bahador,Montazerozohori, Morteza,Habibi, Mohammad Hossein,Zolfigol, Mohammad Ali

, p. 513 - 516 (2005)

Neat chlorosulfonic acid reacts with anhydrous sodium tungstate to give tungstate sulfuric acid (TSA) as a new two basic inorganic solid acid in which two sulfuric acid connect to tungstate moiety via covalent bond. Hantzsch 1, 4-dihydro pyridines (1, 4-D

Oxidation of Hantzsch esters, by means of the new HNO3/bentonite system, and irradiation in a microwave oven

Garcia,Delgado,Cano,Alvarez

, p. 623 - 625 (1993)

We report the aromatization of 1,4-dihydropyridines on using the system HNO3/Bentonite in absence of solvent, by irradiation of the samples in a microwave oven, obtaining excellent yields on very short times comparing with the normal procedures.

Biomimetic oxidation of Hantzsch 1,4-dihydropyridines with tetra-n-butylammonium periodate catalyzed by tetraphenylporphyrinatomanganese(III) chloride [Mn(TPP)Cl]

Nasr-Esfahani, Masoud,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah

, p. 3276 - 3278 (2005)

Efficient oxidation of Hantzsch 1,4-dihydropyridines to their corresponding pyridine derivatives with (Bu4N)IO4 catalyzed by tetraphenylporphyrinatomanganese(III) chloride [Mn(TPP)Cl] is reported. This catalytic system shows high eff

Efficient oxidation of Hantzsch 1,4-dihydropyridines with nicotinium dichromate

Sadeghi,Mohammadpoor-Baltork,Memarian,Sobhani

, p. 1661 - 1665 (2000)

A convenient method for the oxidation of various 4-substituted Hantzsch 1,4-dihydropyridines with nicotinium dichromate (NDC) in refluxing acetonitrile is reported. The yields obtained are excellent.

Chemoselective oxidation of 1,4-dihydropyridines with [NO+.Crown.H(NO3)2-]

Zolfigol, Mohammad Ali,Zebarjadian, Mohammad Hassan,Sadegh, Majid M.,Mohammadpoor-Baltork, Iraj,Memarian, Hamid Reza,Shamsipur, Mojtaba

, p. 929 - 934 (2001)

An ionic complex has been obtained from N2O4 in the presence of the macrocyclic ether 18-crown-6. This crystalline compound was used as an effective oxidizing agent for the oxidation of dihydropyridines to their corresponding pyridin

Application of silica vanadic acid [SiO2-VO(OH)2] as a heterogeneous and recyclable catalyst for oxidative aromatization of Hantzsch 1,4-dihydropyridines at room temperature

Safaiee, Maliheh,Zolfigol, Mohammad Ali,Tavasoli, Mahsa,Mokhlesi, Mohammad

, p. 1593 - 1597 (2014)

A simple method for the oxidative aromatization of Hantzsch 1,4-dihydropyridines to the corresponding pyridines is described using hydrogen peroxide as green oxidant and silica vanadic acid as catalyst in acetonitrile at room temperature. The catalyst can

Catalytic aromatization of hantzsch 1, 4-dihydropyridines by bis (salicylaldehyde-1, 2-phenylenediimine) Mn (III) chloride using urea hydrogen peroxide as mild and efficient oxidant

Karami, Bahador,Montazerozohori, Morteza,Nasr-Esfahani, Masoud

, p. 2181 - 2188 (2005)

A variety of Hantzsch 1,4-dihyropyridines were oxidized efficiently by a catalytic amount of bis(salicylaldehyde-1,2-phenylenediimine)Mn(III) chloride (Mn(III)-salophen I) in the presence of urea hydrogen peroxide adduct (UHP II) as convenient and mild ox

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