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1415262-29-1

2-tert-butyl-2,3-dihydroquinolin-4(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415262-29-1 Structure

  • Basic information

    1. Product Name: 2-tert-butyl-2,3-dihydroquinolin-4(1H)-one
    2. Synonyms: 2-tert-butyl-2,3-dihydroquinolin-4(1H)-one
    3. CAS NO:1415262-29-1
    4. Molecular Formula:
    5. Molecular Weight: 279.382
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415262-29-1.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: 2-tert-butyl-2,3-dihydroquinolin-4(1H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-tert-butyl-2,3-dihydroquinolin-4(1H)-one(1415262-29-1)
    11. EPA Substance Registry System: 2-tert-butyl-2,3-dihydroquinolin-4(1H)-one(1415262-29-1)

  • 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: 1415262-29-1(Hazardous Substances Data)

1415262-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415262-29-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,2,6 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1415262-29:
(9*1)+(8*4)+(7*1)+(6*5)+(5*2)+(4*6)+(3*2)+(2*2)+(1*9)=131
131 % 10 = 1
So 1415262-29-1 is a valid CAS Registry Number.

1415262-29-1Downstream Products

1415262-29-1Relevant articles and documents

The cyclisation of 2'-aminochalcones using silica-supported Yb(OTf)3 under solvent-free conditions

Li, Jianjun,Jin, Linyong,Yu, Chuanming,Su, Weike

, p. 170 - 173 (2009)

Silica-supported Yb(OTf)3 is utilised as a catalyst for the synthesis of 2-substituted dihydroquinolinones from 2'-amino chalcones in good yields. The catalyst is easily prepared and is active under solvent-free conditions and environmentally friendly con

Organometallic titanocene complex as highly efficient bifunctional catalyst for intramolecular Mannich reaction

Wang, Yunyun,Jian, Yajun,Wu, Ya,Sun, Huaming,Zhang, Guofang,Zhang, Weiqiang,Gao, Ziwei

, (2019/05/07)

Bifunctional catalysts bearing two catalytic sites, Lewis acidic organometallic titanocene and Br?nsted acidic COOH, have been assembled in situ from Cp2TiCl2 with carboxylic acid ligands, showing high catalytic activity over an intramolecular Mannich reaction towards synthesis of 2-aryl-2,3-dihydroquinolin-4(1H)-ones. The determination of the bifunctional catalyst Cp2Ti(C8H4NO6)2 was elucidated by single X-ray HR-MS and investigation of catalytic behavior. In particular, masking the Br?nsted acidic COOH catalytic site with dormant COOMe lowered the reaction yield greatly, indicating that two catalytic sites work together to maintain high catalytic efficiency.

Titanocene complex with oxygen-containing carboxylic acid as ligand as well as preparation method and application of titanocene complex

-

Paragraph 0039; 0040; 0042, (2018/11/03)

The invention discloses a titanocene complex with oxygen-containing carboxylic acid as well as a preparation method and an application of the titanocene complex. The structural formula of the complexis shown in the description. The titanocene complex is p

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