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130186-64-0

9-AMINO-3,3-DIMETHYL-3,4-DIHYDRO-1(2H)-ACRIDINONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130186-64-0 Structure

  • Basic information

    1. Product Name: 9-AMINO-3,3-DIMETHYL-3,4-DIHYDRO-1(2H)-ACRIDINONE
    2. Synonyms: 9-AMINO-3,3-DIMETHYL-3,4-DIHYDRO-1(2H)-ACRIDINONE;9-Amino-3,3-dimethyl-3,4-dihydro-2H-acridin-1-one;9-amino-3,3-dimethyl-3,4-dihydroacridin-1(2H)-one
    3. CAS NO:130186-64-0
    4. Molecular Formula: C15H16N2O
    5. Molecular Weight: 240.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130186-64-0.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: 9-AMINO-3,3-DIMETHYL-3,4-DIHYDRO-1(2H)-ACRIDINONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-AMINO-3,3-DIMETHYL-3,4-DIHYDRO-1(2H)-ACRIDINONE(130186-64-0)
    11. EPA Substance Registry System: 9-AMINO-3,3-DIMETHYL-3,4-DIHYDRO-1(2H)-ACRIDINONE(130186-64-0)

  • 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: 130186-64-0(Hazardous Substances Data)

130186-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130186-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130186-64:
(8*1)+(7*3)+(6*0)+(5*1)+(4*8)+(3*6)+(2*6)+(1*4)=100
100 % 10 = 0
So 130186-64-0 is a valid CAS Registry Number.

130186-64-0Downstream Products

130186-64-0Relevant articles and documents

Synthesis of 4-methyl-2,3-disubstituted quinoline scaffolds via environmentally benign Fe(iii) catalysed sequential condensation, cyclization and aromatization of 1,3-diketone and 2-ethynylaniline

Sivaraman, Mahalingam,Perumal, Paramasivan T.

, p. 52060 - 52066 (2014/12/10)

Environmentally benign Fe(iii)-catalysed sequential condensation, cyclization and aromatization of 1,3-diketone and 2-ethynylaniline derivatives to the substituted quinoline scaffolds with good to excellent yield in shorter reaction time is described. This journal is

Sulfuric acid-modified PEG-6000 (PEG-OSO3H): An efficient, bio-degradable and reusable polymeric catalyst for the solvent-free synthesis of poly-substituted quinolines under microwave irradiation

Hasaninejad, Alireza,Zare, Abdolkarim,Shekouhy, Mohsen,Ameri-Rad, Javad

experimental part, p. 958 - 964 (2011/05/12)

Sulfuric acid-modified polyethylene glycol 6000 (PEG-OSO3H) is applied as an efficient and eco-friendly polymeric catalyst for Friedlaender synthesis of poly-substituted quinolines from 2-aminoaryl ketones (or anthranilonitrile) and carbonyl compounds possessing a reactive methylene group under microwave irradiation and solvent-free conditions. The reactions are completed in short times, and the products are obtained in good to excellent yields. The Royal Society of Chemistry.

Synthesis and crystal structure of 7,8-dihydroquinolino[2,3-a]acridine derivatives

Han, Guang-Fan,Wang, Rui-Hua,Zhang, Wen-Tao,Zhao, Yu-Yuan,Xing, Zheng,Dai, Wei

experimental part, p. 2492 - 2505 (2009/12/06)

Novel 9-amino-3-substituted-1,2,3,4-acridin-1-one derivatives and 9,14-diamino-7-substituted-7,8-dihydroquinolino[2,3-a]acridine derivatives were synthesized by the condensation reaction of 5-substituted-1,3-cyclohexanedione with 2-aminobenzonitrile and s

9-aminoacridine derivatives possessing psychotropic, antiamnestic and lipid-regulative activity

-

, (2008/06/13)

"Derivatives of 9-aminoacridine characterized by psychothropic, antiamnestic and lipid-regulating activities". New chemical compounds derived of 9-aminoacridine with a general formula are presented: STR1 where R=H or CH3 R1 =H, CHsu

DERIVATIVES OF 9-AMINOACRIDINE HAVING PSYCHOTROPIC, ANTIAMNESTIC AND LIPID REGULATING PROPERTIES

-

, (2008/06/13)

New chemical compounds, derivatives of 9-aminoacridine of general formula (I) where R = H, CH3; R1 = H, CH3, Br; R2 = H, CH3; R3 = alkyl-C1-C5, arylmethyl, diethylaminoethyl; X = C = O, CHOH; Y = CH2; X + Y = CH = CH; and their salts with organic and non-organic acids. The desired compounds are obtained by interaction of substituted nitriles of antranyl acid with dimedone with subsequent cyclization of intermediate enaminonitriles into corresponding ketones of 9-aminoacridine after the reduction of which and of their derivatives alkylated or aralkylated on the 9-amino group, the corresponding alcohols are obtained, after hydration of which 9-amino-3,4-dihydroacridines are obtained. When experimented on animals, the said derivatives of 9-aminoacridine have shown psychotropic, antiamnestic and lipid regulating properties, as well as a lower toxicity in comparison with known preparations.

Acridine derivatives

-

, (2008/06/13)

A compound of the formula : wherein R1 is hydrogen, halogen, hydroxy, lower alkoxy, lower alkyl or mono(or di or tri)halo(lower)alkyl, and (in which R2 and R3 are each lower alkyl),and a pharmaceutically acceptable salt thereof, processes for their prepar

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