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[3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine is an amine compound that features a substituted isoxazolyl ring and a methyloxyphenyl group. It is a derivative of the phenylamine class of compounds, and the presence of the isoxazolyl and methyloxy groups endows it with unique chemical and biological properties. [3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine may hold potential applications across various sectors, including pharmaceuticals, agrochemicals, and materials science, with its specific uses and properties being subject to further research and development.

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  • 1300031-61-1 Structure
  • Basic information

    1. Product Name: [3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine
    2. Synonyms: [3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine;3-(3,5-dimethylisoxazol-4-yl)-4-methoxyaniline
    3. CAS NO:1300031-61-1
    4. Molecular Formula: C12H14N2O2
    5. Molecular Weight: 218.25176
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1300031-61-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 343.3±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.151±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.55±0.10(Predicted)
    10. CAS DataBase Reference: [3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine(CAS DataBase Reference)
    11. NIST Chemistry Reference: [3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine(1300031-61-1)
    12. EPA Substance Registry System: [3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine(1300031-61-1)
  • 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: 1300031-61-1(Hazardous Substances Data)

1300031-61-1 Usage

Uses

Used in Pharmaceutical Industry:
[3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine is used as a potential active pharmaceutical ingredient for [application reason] due to its unique chemical structure and biological properties.
Used in Agrochemical Industry:
In the agrochemical industry, [3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine is used as a [application type] for [application reason], leveraging its specific chemical and biological characteristics.
Used in Materials Science:
[3-(3,5-diMethyl-4-isoxazolyl)-4-(Methyloxy)phenyl]aMine is utilized as a [application type] in materials science for [application reason], taking advantage of its distinctive properties.
(Note: The "application type" and "application reason" would need to be filled in with specific details based on the compound's properties and potential uses once they are identified through further research and development.)

Check Digit Verification of cas no

The CAS Registry Mumber 1300031-61-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,0,0,3 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1300031-61:
(9*1)+(8*3)+(7*0)+(6*0)+(5*0)+(4*3)+(3*1)+(2*6)+(1*1)=61
61 % 10 = 1
So 1300031-61-1 is a valid CAS Registry Number.

1300031-61-1Relevant articles and documents

METHODS AND COMPOUNDS FOR THE TREATMENT OF GENETIC DISEASE

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Paragraph 00616; 00754; 00757; 00758, (2021/08/13)

The present disclosure relates to compounds and methods for modulating the expression of dmpk, and treating diseases and conditions in which dmpk plays an active role. The compound can be a transcription modulator molecule having a first terminus, a second terminus, and oligomeric backbone, wherein: a) the first terminus comprises a DNA-binding moiety capable of noncovalently binding to a nucleotide repeat sequence CAG or CTG; b) the second terminus comprises a protein-binding moiety binding to a regulatory molecule that modulates an expression of a gene comprising the nucleotide repeat sequence CAG or CTG; and c) the oligomeric backbone comprising a linker between the first terminus and the second terminus.

QUINOLINE DERIVATIVES AS BROMODOMAIN INHIBITORS

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Page/Page column 26; 27, (2016/12/07)

Provided is a novel quinoline derivative inhibiting the bromodomain and extra terminal domain (BET) proteins, and a pharmaceutical composition comprising the same which can be useful for prevention or treatment of a precancerous transformation or a cancer.

OXAZOLO[5,4-C]QUINOLIN-2-ONE COMPOUNDS AS BROMODOMAIN INHIBITORS

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Paragraph 00231, (2014/10/04)

The present invention relates to compounds useful as bromodomain inhibitors. The invention also provides pharmaceutically acceptable compositions comprising compounds of the present invention and methods of using said compounds and compositions in the treatment of various diseases and disorders.

7-(3,5-Dimethyl-4-Isoxazolyl)-8-(Methyloxy)-1H-Imidazo[4,5-C]Quinoline Derivatives

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Paragraph 0180-0181, (2014/03/21)

Novel quinoline compounds pharmaceutical compositions containing such compounds and their use in therapy.

4-(8-METHOXY-1-((1-METHOXYPROPAN-2-YL)-2-(TETRAHYDRO-2H-PYRAN-4-YL)-1 H-IMIDAZO[4,5-C]QUINOLIN-7-YL)-3,5-DIMETHYLISOXAZOLE AND ITS USE AS BROMODOMAIN INHIBITOR

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, (2013/03/26)

Novel quinoline compounds of formula (I), pharmaceutical compositions containing such compounds and their use in therapy, as bromodomain inhibitors.

From ApoA1 upregulation to BET family bromodomain inhibition: Discovery of I-BET151

Mirguet, Olivier,Lamotte, Yann,Donche, Frédéric,Toum, Jér?me,Gellibert, Franoise,Bouillot, Anne,Gosmini, Romain,Nguyen, Van-Loc,Delannée, Delphine,Seal, Jonathan,Blandel, Florence,Boullay, Anne-Bénédicte,Boursier, Eric,Martin, Sandrine,Brusq, Jean-Marie,Krysa, Gael,Riou, Alizon,Tellier, Rémi,Costaz, Agns,Huet, Pascal,Dudit, Yann,Trottet, Lionel,Kirilovsky, Jorge,Nicodeme, Edwige

supporting information; experimental part, p. 2963 - 2967 (2012/06/04)

The discovery, synthesis and biological evaluation of a novel series of 7-isoxazoloquinolines is described. Several analogs are shown to increase ApoA1 expression within the nanomolar range in the human hepatic cell line HepG2.

NOVEL COMPOUNDS

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Page/Page column 32, (2012/11/07)

Novel quinoline compounds pharmaceutical compositions containing such compounds and their use in therapy.

Imidazo [4, 5-C] Quinoline Derivatives As Bromodomain Inhibitors

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Page/Page column 18, (2012/09/22)

Novel compounds of formula (I) and salts thereof, pharmaceutical compositions containing such compounds and their use in therapy.

IMIDAZO [4, 5-C] QUINOLINE DERIVATES AS BROMODOMAIN INHIBITORS

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Page/Page column 42, (2011/06/11)

Novel compounds of Formula (I) and salts thereof, pharmaceutical compositions containing such compounds and their use in therapy.

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