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1H-Isoindole-1,3(2H)-dione, 2-[[(2-methoxyphenyl)thio]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 849363-80-0 Structure
  • Basic information

    1. Product Name: 1H-Isoindole-1,3(2H)-dione, 2-[[(2-methoxyphenyl)thio]methyl]-
    2. Synonyms:
    3. CAS NO:849363-80-0
    4. Molecular Formula: C16H13NO3S
    5. Molecular Weight: 299.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 849363-80-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Isoindole-1,3(2H)-dione, 2-[[(2-methoxyphenyl)thio]methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Isoindole-1,3(2H)-dione, 2-[[(2-methoxyphenyl)thio]methyl]-(849363-80-0)
    11. EPA Substance Registry System: 1H-Isoindole-1,3(2H)-dione, 2-[[(2-methoxyphenyl)thio]methyl]-(849363-80-0)
  • 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: 849363-80-0(Hazardous Substances Data)

849363-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849363-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,3,6 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 849363-80:
(8*8)+(7*4)+(6*9)+(5*3)+(4*6)+(3*3)+(2*8)+(1*0)=210
210 % 10 = 0
So 849363-80-0 is a valid CAS Registry Number.

849363-80-0Relevant articles and documents

Access to the new isoindolo[1,3]benzothiazocinones via the combination of N-acyliminium chemistry and friedel-crafts type π-cyclization

Cul, Armelle,Daich, Adam,Decroix, Bernard,Sanz, Gerard,Van Hijfte, Luc

, p. 33 - 39 (2004)

New racemic and chiral [4,2]- and [3,5]benzothiazocines (4) and (5) in the isoindolinone series were synthesized easily in few steps based on the combination of N-acyliminium chemistry and π-cationic cyclization of acylium ions. The chemoselectivity observed during these processes, particularly in the reduction, the thioalkylation and the cyclization stages, were also discussed.

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