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CAS

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1330527-03-1

methyl 2-methyl-5,10-dioxo-4-phenyl-1,4,5,10-tetrahydrobenzo[g]quinoline-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1330527-03-1 Structure

  • Basic information

    1. Product Name: methyl 2-methyl-5,10-dioxo-4-phenyl-1,4,5,10-tetrahydrobenzo[g]quinoline-3-carboxylate
    2. Synonyms: methyl 2-methyl-5,10-dioxo-4-phenyl-1,4,5,10-tetrahydrobenzo[g]quinoline-3-carboxylate
    3. CAS NO:1330527-03-1
    4. Molecular Formula:
    5. Molecular Weight: 359.381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1330527-03-1.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: methyl 2-methyl-5,10-dioxo-4-phenyl-1,4,5,10-tetrahydrobenzo[g]quinoline-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-methyl-5,10-dioxo-4-phenyl-1,4,5,10-tetrahydrobenzo[g]quinoline-3-carboxylate(1330527-03-1)
    11. EPA Substance Registry System: methyl 2-methyl-5,10-dioxo-4-phenyl-1,4,5,10-tetrahydrobenzo[g]quinoline-3-carboxylate(1330527-03-1)

  • 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: 1330527-03-1(Hazardous Substances Data)

1330527-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1330527-03-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,0,5,2 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1330527-03:
(9*1)+(8*3)+(7*3)+(6*0)+(5*5)+(4*2)+(3*7)+(2*0)+(1*3)=111
111 % 10 = 1
So 1330527-03-1 is a valid CAS Registry Number.

1330527-03-1Downstream Products

1330527-03-1Relevant articles and documents

Synthesis of Tetrahydrobenzo[g]Quinoline Derivatives Using Recoverable Carbonaceous Material as Heterogeneous Catalyst

Lin, Jialing,Chen, Jiameng,Ji, Hongfu,Zhao, Jun,Zhang, Furen,Li, Chunmei

, p. 2022 - 2028 (2017)

A variety of substituted benzo[g]quinoline-5,10-dione derivatives were synthesized via one-pot three-component reaction of 2-hydroxynaphthalene-1,4-dione, aromatic aldehydes, and (E)-3-aminobut-2-enoates using carbonaceous material as the heterocyclic catalyst. This procedure is simple and efficient owing to short reaction times, easy work-up, and recovery of heterogeneous catalyst. This procedure develops an efficient and promising synthetic method to construction of the benzo[g]quinoline-5,10-dione skeleton.

Facile, four-component, domino reactions for the regioselective synthesis of tetrahydrobenzo[g]quinolines

Devi Bala, Balasubramanian,Balamurugan, Kamaraj,Perumal, Subbu

supporting information; experimental part, p. 4562 - 4566 (2011/09/20)

Facile, four-component domino reactions of 2-hydroxy-1,4-naphthaquinone, aromatic aldehydes, methyl/ethyl acetoacetate and ammonium acetate in ethanol under microwave irradiation at 100 °C afforded tetrahydrobenzo[g]quinoline- 5,10-diones regioselectively

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