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486994-31-4

5-bromo-3-hydroxy-1-methyl-3-(2-oxo-2-phenylethyl)-1,3-dihydro-2H-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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  • 486994-31-4 Structure

  • Basic information

    1. Product Name: 5-bromo-3-hydroxy-1-methyl-3-(2-oxo-2-phenylethyl)-1,3-dihydro-2H-indol-2-one
    2. Synonyms: 5-bromo-3-hydroxy-1-methyl-3-(2-oxo-2-phenylethyl)-1,3-dihydro-2H-indol-2-one
    3. CAS NO:486994-31-4
    4. Molecular Formula: C17H14BrNO3
    5. Molecular Weight: 360.20196
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 486994-31-4.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: 5-bromo-3-hydroxy-1-methyl-3-(2-oxo-2-phenylethyl)-1,3-dihydro-2H-indol-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-bromo-3-hydroxy-1-methyl-3-(2-oxo-2-phenylethyl)-1,3-dihydro-2H-indol-2-one(486994-31-4)
    11. EPA Substance Registry System: 5-bromo-3-hydroxy-1-methyl-3-(2-oxo-2-phenylethyl)-1,3-dihydro-2H-indol-2-one(486994-31-4)

  • 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: 486994-31-4(Hazardous Substances Data)

486994-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 486994-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,9,9 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 486994-31:
(8*4)+(7*8)+(6*6)+(5*9)+(4*9)+(3*4)+(2*3)+(1*1)=224
224 % 10 = 4
So 486994-31-4 is a valid CAS Registry Number.

486994-31-4Downstream Products

486994-31-4Relevant articles and documents

Autoxidation/Aldol Tandem Reaction of 2-Oxindoles with Ketones: A Green Approach for the Synthesis of 3-Hydroxy-2-Oxindoles

Zhang, Qing-Bao,Jia, Wen-Liang,Ban, Yong-Liang,Zheng, Yong,Liu, Qiang,Wu, Li-Zhu

, p. 2595 - 2598 (2016/02/27)

In the presence of tetrabutylammonium fluoride and molecular sieves (MS) 4 ? in DMF, an efficient autoxidation reaction of 2-oxindoles with ketones under air at room temperature has been developed. This approach may provide a green, practical, and metal-free protocol for a wide range of biologically important 3-hydroxy-3-(2-oxo-alkyl)-2-oxindoles.

Catalytic asymmetric synthesis of substituted 3-hydroxy-2oxindoles

Hanhan, Nadine V.,Sahin, Aziza H.,Chang, Toby W.,Fettinger, James C.,Franz, Annaliese K.

supporting information; experimental part, p. 744 - 747 (2010/04/06)

Chemical equation presented Chemical equation presented No more double trouble: The competing double-addition pathway was suppressed when chiral scandium(III) and indium (III) complexes were used to catalyze the addition of indoles and other π nucleophile

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