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Ethanone, 1-(2,3-dihydrofuro[2,3-b]pyridin-6-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 253874-76-9 Structure
  • Basic information

    1. Product Name: Ethanone, 1-(2,3-dihydrofuro[2,3-b]pyridin-6-yl)- (9CI)
    2. Synonyms: Ethanone, 1-(2,3-dihydrofuro[2,3-b]pyridin-6-yl)- (9CI)
    3. CAS NO:253874-76-9
    4. Molecular Formula: C9H9NO2
    5. Molecular Weight: 163.17326
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP
    8. Mol File: 253874-76-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 312.5±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.214±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.01±0.20(Predicted)
    10. CAS DataBase Reference: Ethanone, 1-(2,3-dihydrofuro[2,3-b]pyridin-6-yl)- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Ethanone, 1-(2,3-dihydrofuro[2,3-b]pyridin-6-yl)- (9CI)(253874-76-9)
    12. EPA Substance Registry System: Ethanone, 1-(2,3-dihydrofuro[2,3-b]pyridin-6-yl)- (9CI)(253874-76-9)
  • 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: 253874-76-9(Hazardous Substances Data)

253874-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253874-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,8,7 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 253874-76:
(8*2)+(7*5)+(6*3)+(5*8)+(4*7)+(3*4)+(2*7)+(1*6)=169
169 % 10 = 9
So 253874-76-9 is a valid CAS Registry Number.

253874-76-9Downstream Products

253874-76-9Relevant articles and documents

1,2,4-Triazines in organic synthesis. 8. Intramolecular diels-alder reaction of 5-acyl-1,2,4-triazineoxime ethers. New route of synthesis of alkylhetarylketones

Lipinska,Branowska,Rykowski

, p. 334 - 342 (1999)

Intramolecular diene cycloaddition of 5-acyl-1,2,4-triazineoxime ethers involving a dienophile substituent in the 3-position of the triazine ring is studied. New alkylhetarylketones are synthesized by hydrolysis of the condensed N- and O-containing hetero

2,3-DIHYDROFURO[2,3-B]PYRIDINE COMPOUNDS

-

, (2020/01/11)

The present invention provides a compound of Formula I: wherein R is H or F; or a pharmaceutically acceptable salt thereof, and the use of compounds of Formula I for treatment of neurodegenerative diseases, such as Alzheimer's disease.

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