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5-fluoro-1,3-dihydro-3-[(4-methoxyphenyl)imino]-2H-indole-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1326527-34-7 Structure
  • Basic information

    1. Product Name: 5-fluoro-1,3-dihydro-3-[(4-methoxyphenyl)imino]-2H-indole-2-one
    2. Synonyms: 5-fluoro-1,3-dihydro-3-[(4-methoxyphenyl)imino]-2H-indole-2-one
    3. CAS NO:1326527-34-7
    4. Molecular Formula:
    5. Molecular Weight: 270.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1326527-34-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.32±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-fluoro-1,3-dihydro-3-[(4-methoxyphenyl)imino]-2H-indole-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-fluoro-1,3-dihydro-3-[(4-methoxyphenyl)imino]-2H-indole-2-one(1326527-34-7)
    11. EPA Substance Registry System: 5-fluoro-1,3-dihydro-3-[(4-methoxyphenyl)imino]-2H-indole-2-one(1326527-34-7)
  • 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: 1326527-34-7(Hazardous Substances Data)

1326527-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1326527-34-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,6,5,2 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1326527-34:
(9*1)+(8*3)+(7*2)+(6*6)+(5*5)+(4*2)+(3*7)+(2*3)+(1*4)=147
147 % 10 = 7
So 1326527-34-7 is a valid CAS Registry Number.

1326527-34-7Relevant articles and documents

"On water" synthesis of spiro-indoles via Schiff bases

Panda, Siva S.,Jain, Subhash C.

experimental part, p. 1187 - 1194 (2012/09/25)

A fast, efficient, and clean "on water" synthesis of new Schiff bases and their conversion to spiro compounds under microwave irradiation, as well as in water, is reported. Indol-2,3-diones were reacted separately with various heterocyclic and aromatic am

Synthesis of 1′-aryl-2′-(2-oxoindolin-3-yl)spiro[indoline-3, 5′-pyrroline]-2,3′-dione via one-pot reaction of arylamines, acetone, and isatins

Sun, Yan,Sun, Jing,Yan, Chao-Guo

supporting information; experimental part, p. 3647 - 3649 (2012/09/22)

An efficient synthetic method for 1′-aryl-2′-(2-oxoindolin-3- yl)spiro[indoline-3,5′-pyrroline]-2,3′-diones was successfully developed via the one-pot domino reaction of arylamines, acetone, and isatins in acetic acid. The reaction mechanism involved the

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