Welcome to LookChem.com Sign In|Join Free

CAS

  • or

117519-07-0

3-Nitro-6-(trifluoromethyl)pyridin-2(1H)-one is a chemical compound belonging to the class of organofluorides and nitro compounds. It features a distinctive six-membered Pyridine ring structure, which is further functionalized with a nitro group and a trifluoromethyl group. 3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one is known for its unique reactivity and is widely utilized in chemical and pharmaceutical research due to its versatile applications. However, its physical properties and potential toxicity, safety concerns, or environmental impact are not well-documented, necessitating careful handling and disposal.

117519-07-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 117519-07-0 Structure

  • Basic information

    1. Product Name: 3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one
    2. Synonyms: 3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one;3-Nitro-6-(trifluoroMethyl)pyridin-2-ol;2-Hydroxy-3-nitro-6-(trifluoromethyl)pyridine
    3. CAS NO:117519-07-0
    4. Molecular Formula: C6H3F3N2O3
    5. Molecular Weight: 208.0948296
    6. EINECS: N/A
    7. Product Categories: nitro-compound
    8. Mol File: 117519-07-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 278.6±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: Light yellow liquid
    5. Density: 1.61±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 4.38±0.10(Predicted)
    10. CAS DataBase Reference: 3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one(117519-07-0)
    12. EPA Substance Registry System: 3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one(117519-07-0)

  • 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: 117519-07-0(Hazardous Substances Data)

117519-07-0 Usage

Uses

Used in Chemical Research:
3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one is used as a research chemical for its unique reactivity and potential applications in the synthesis of various organic compounds.
Used in Pharmaceutical Research:
3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one is used as a pharmaceutical intermediate for the development of new drugs, given its versatile chemical properties and potential to be modified for specific therapeutic applications.
Used in the Synthesis of Active Pharmaceutical Ingredients (APIs):
3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one is used as a key building block in the synthesis of APIs, particularly those targeting specific biological pathways or receptors.
Used in the Development of Agrochemicals:
3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one is used as a starting material in the development of agrochemicals, such as pesticides and herbicides, due to its potential to be modified for specific pesticidal or herbicidal properties.
Used in the Synthesis of Advanced Materials:
3-Nitro-6-(trifluoroMethyl)pyridin-2(1H)-one is used as a precursor in the synthesis of advanced materials, such as polymers, dyes, and sensors, owing to its unique chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 117519-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,5,1 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117519-07:
(8*1)+(7*1)+(6*7)+(5*5)+(4*1)+(3*9)+(2*0)+(1*7)=120
120 % 10 = 0
So 117519-07-0 is a valid CAS Registry Number.

117519-07-0Relevant articles and documents

HMOX1 inducers

-

Page/Page column 150, (2020/09/18)

The present invention is related to compounds of structure (I) as heme oxygenase 1 (HMOX 1) inducers. The present invention is also related a method of controlling the activity or the amount, or both the activity and the amount, of heme-oxygenase 1 in a mammalian subject. The definitions of the variables are provided herein.

NITROGENATED HETEROCYCLIC COMPOUND

-

Paragraph 0651, (2015/03/28)

The present invention provides a compound having a PDE2A selective inhibitory action, which is useful as an agent for the prophylaxis or treatment of schizophrenia, Alzheimer's disease and the like. The present invention is a compound represented by the formula (1): wherein each symbol is as described in the specification, or a salt thereof.

Non-nucleoside reverse transcriptase inhibitors

-

, (2008/06/13)

Provided are compounds of the general formula I: wherein R2 is selected from the group consisting of H, F, Cl, (C1-4) alkyl, (C3-4) cycloalkyl and CF3; R4 is H or Me; R5 is H, Me or Et, wit

C6 modification of the pyridinone core of thrombin inhibitor L-374,087 as a means of enhancing its oral absorption

Isaacs, Richard C. A.,Cutrona, Kellie J.,Newton, Christina L.,Sanderson, Philip E. J.,Solinsky, Mark G.,Baskin, Elizabeth P.,Chen, I-Wu,Cooper, Carolyn M.,Cook, Jacquelynn J.,Gardell, Stephen J.,Lewis, S. Dale,Lucas Jr., Robert J.,Lyle, Elizabeth A.,Lynch Jr., Joseph J.,Naylor-Olsen, Adel M.,Stranieri, Maria T.,Vastag, Kari,Vacca, Joseph P.

, p. 1719 - 1724 (2007/10/03)

1 (L-374,087) is a potent, selective, efficacious, and orally bioavailable thrombin inhibitor that contains a core 3-amino-2-pyridinone moiety. Replacement of the C6 pyridinone metyl group of 1 by a propyl group gave 5 (L-375,052), which retained all the excellent properties of 1, and also yielded higher plasma levels after oral dosing in dogs and rats.

PYRIDINONE THROMBIN INHIBITORS

-

, (2008/06/13)

Compounds of the invention are useful in inhibiting thrombin and associated thrombotic occlusions and have the following structure: STR1 for example: STR2

Synthesis of substituted azaoxindoles for the preparation of aza-tenidap analogs

Robinson, Ralph P.,Donahue, Kathleen M.,Son, Paul S.,Wagy, Steven D.

, p. 287 - 293 (2007/10/03)

The preparation of a set of eight azaoxindoles bearing substituents on the aromatic nucleus is outlined. These compounds were required for the preparation of aza-analogs of the anti-inflammatory oxindole tenidap. Two methods of synthesis were used, the fi

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 117519-07-0