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Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)(9CI) is a heterocyclic chemical compound characterized by the fusion of a pyrazine and a pyridine ring, with an additional isopropyl group. It is classified as a pyrazinone and has the molecular formula C11H10N2O. Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)(9CI) is primarily utilized in the research and development of pharmaceuticals and organic synthesis, with its potential applications in the pharmaceutical industry being attributed to its unique structural features.

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  • 179123-09-2 Structure
  • Basic information

    1. Product Name: Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)- (9CI)
    2. Synonyms: Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)- (9CI);3-(1-METHYLETHYL)PYRIDO[2,3-B]PYRAZIN-2(1H)-ONE
    3. CAS NO:179123-09-2
    4. Molecular Formula: C10H11N3O
    5. Molecular Weight: 189.21384
    6. EINECS: N/A
    7. Product Categories: PIPERIDINE
    8. Mol File: 179123-09-2.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: Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)- (9CI)(179123-09-2)
    11. EPA Substance Registry System: Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)- (9CI)(179123-09-2)
  • 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: 179123-09-2(Hazardous Substances Data)

179123-09-2 Usage

Uses

Used in Pharmaceutical Research and Development:
Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)(9CI) is employed as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)(9CI) serves as a valuable building block for the creation of more complex organic molecules. Its reactivity and structural properties make it a versatile component in the synthesis of a wide range of organic compounds.
Used in Drug Design:
Due to its heterocyclic nature and the presence of a pyrazinone moiety, Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)(9CI) is used in drug design to explore its potential as a lead compound for the development of new pharmaceutical agents. Its structural features may contribute to the modulation of biological targets, offering opportunities for the treatment of various diseases and conditions.
Used in Medicinal Chemistry:
In medicinal chemistry, Pyrido[2,3-b]pyrazin-2(1H)-one, 3-(1-methylethyl)(9CI) is utilized for the investigation of its pharmacological properties and potential therapeutic effects. Its unique structure may provide insights into the design of novel drugs with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 179123-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,1,2 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 179123-09:
(8*1)+(7*7)+(6*9)+(5*1)+(4*2)+(3*3)+(2*0)+(1*9)=142
142 % 10 = 2
So 179123-09-2 is a valid CAS Registry Number.

179123-09-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-propan-2-yl-1H-pyrido[2,3-b]pyrazin-2-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:179123-09-2 SDS

179123-09-2Downstream Products

179123-09-2Relevant articles and documents

Chemical defense of giant springtail Tetrodontophora bielanensis (Waga) (Insecta: Collembola)

Dettner,Scheuerlein,Fabian,Schulz,Francke

, p. 1051 - 1074 (2007/10/03)

The giant springtail, Tetrodontophora bielanensis (Waga), is characterized by integumental openings (pseudocells) from which small droplets of a sticky defensive fluid are secreted after molestation. The secretion originates initially from secretory cells below the pseudocellae; subsequent irritations result in release of hemolymph, which was identified by both chemical and microscopical methods as well as by scanning electron microscopy. Bioassays with topically treated ground beetles Nebria brevicollis showed that the pseudocellular fluid evokes a total disorientation and cleansing behavior of the beetle. The main constituents were identified as the following pyridopyrazines: 2,3- dimethoxpyridol[2,3- h]pyrazine (1), 3-isopropyl-2-methoxypyrid[2,3-b]pyrazine (2), and- 2- methoxy-4H-pyrido[2,3-b]pyrazine-3-one (3). These alkaloids are mainly present in the pseudocellar fluids of female and male springtails but are absent in their food or feces. Minor amounts are found in the hemolymph of adults, while larvae contain traces of 2 only. All compounds were synthesized and tested tot activity. In natural concentrations, the synthetic alkaloids elicited the same effects from the ground beetles as the pseudocellar fluid.

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