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216219-62-4

1-(2,3-DIBROMOPROPYL)-1H-INDOLE-2,3-DIONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 216219-62-4 Structure

  • Basic information

    1. Product Name: 1-(2,3-DIBROMOPROPYL)-1H-INDOLE-2,3-DIONE
    2. Synonyms: 1-(2,3-DIBROMOPROPYL)-1H-INDOLE-2,3-DIONE
    3. CAS NO:216219-62-4
    4. Molecular Formula: C11H9Br2NO2
    5. Molecular Weight: 347
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 216219-62-4.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: 1-(2,3-DIBROMOPROPYL)-1H-INDOLE-2,3-DIONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2,3-DIBROMOPROPYL)-1H-INDOLE-2,3-DIONE(216219-62-4)
    11. EPA Substance Registry System: 1-(2,3-DIBROMOPROPYL)-1H-INDOLE-2,3-DIONE(216219-62-4)

  • 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: 216219-62-4(Hazardous Substances Data)

216219-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216219-62-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,2,1 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 216219-62:
(8*2)+(7*1)+(6*6)+(5*2)+(4*1)+(3*9)+(2*6)+(1*2)=114
114 % 10 = 4
So 216219-62-4 is a valid CAS Registry Number.

216219-62-4Upstream product

216219-62-4Downstream Products

216219-62-4Relevant articles and documents

4-hydroxy-2-quinolones 170. Synthesis and bromination of N-allylisatin

Ukrainets,Bereznyakova,Gorokhova,Shishkina

, p. 1241 - 1247 (2009)

Independently of the reaction conditions N-allylisatin forms only the 2, 3-dibromo derivative upon treatment with molecular bromine in contrast to N-allyl-substituted quinolin- or pyrid-2-ones which readily undergo halocyclization to the corresponding 2-bromomethyl oxazoles.

Syntheses of 1-(2-bromo-3-hydroxypropyl)- and 1-(2-bromo-2-propenyl)isatins and their β-thiosemicarbazones

Rekhter,Rekhter,Yazlovetskii,Panasenko,Makaev

, p. 275 - 277 (1998)

Only the bromine atom at the primary carbon atom participates in nucleophilic replacement by a trifluoroacetate ion and elimination of HBr in 1-(2,3-dibromopropyl)isatin. 1998 Plenum Publishing Corporation.

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