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3-(2-AMINO-BENZYLIDENE)-1,3-DIHYDRO-INDOL-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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  • 17990-71-5 Structure
  • Basic information

    1. Product Name: 3-(2-AMINO-BENZYLIDENE)-1,3-DIHYDRO-INDOL-2-ONE
    2. Synonyms: 3-[(Z)-(2-AMINOPHENYL)METHYLIDENE]-1H-INDOL-2-ONE;3-(2-AMINO-BENZYLIDENE)-1,3-DIHYDRO-INDOL-2-ONE;(3Z)-3-[(2-aminophenyl)methylidene]-1H-indol-2-one
    3. CAS NO:17990-71-5
    4. Molecular Formula: C15H12N2O
    5. Molecular Weight: 236.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17990-71-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 499.8±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.304±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 12.76±0.20(Predicted)
    10. CAS DataBase Reference: 3-(2-AMINO-BENZYLIDENE)-1,3-DIHYDRO-INDOL-2-ONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(2-AMINO-BENZYLIDENE)-1,3-DIHYDRO-INDOL-2-ONE(17990-71-5)
    12. EPA Substance Registry System: 3-(2-AMINO-BENZYLIDENE)-1,3-DIHYDRO-INDOL-2-ONE(17990-71-5)
  • 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: 17990-71-5(Hazardous Substances Data)

17990-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17990-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,9 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17990-71:
(7*1)+(6*7)+(5*9)+(4*9)+(3*0)+(2*7)+(1*1)=145
145 % 10 = 5
So 17990-71-5 is a valid CAS Registry Number.

17990-71-5Downstream Products

17990-71-5Relevant articles and documents

Studies of the reactions between indole-2,3-diones (isatins) and 2-aminobenzylamine

Bergman, Jan,Engqvist, Robert,St?lhandske, Claes,Wallberg, Hans

, p. 1033 - 1048 (2007/10/03)

Reflux of equimolecular amounts 2-aminobenzylamine and isatins in acetic acid produced indolo[3,2-c]quinolin-6-ones in good yields. A proposed mechanism involving initial formation of a spiro compound is given. This isolable intermediate subsequently rearranges via a sequential isocyanate ring opening and a cyclisation process to a urea derivative which finally cyclized to the indolo[3,2-c]quinolin-6-ones. The urea derivative could be prepared separately and cyclized selectively to indolo[3,2-c]quinolin-6-one. Reaction of N-acetylisatin with 2-aminobenzylamine at room temperature yielded the 1,4-benzodiazepinone 3-(2-acetamidophenyl)-1,5-dihydro-1,4-benzodiazepin-2-one whereas its isomer 2(2-acetamidophenyl)-4,5-dihydro-1,4-benzodiazepin-3-one was obtained from 2-(2-acetylaminophenyl)-N-(2-aminobenzyl)-2-oxoacetamide in acetic acid at room temperature. The previously unknown linear isomer of indolo[3,2-c]quinolin-6-one, i.e. indolo[2,3-b]quinolin-11-one, has been prepared by thermal (260°C) cyclization of methyl 2-phenylamino indole-3-carboxylate, which in turn was prepared in two steps from methyl indole-3-carboxylate.

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