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5-(1-adamantyl)-2-(4-methoxyphenyl)-1H-isoindole-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 303114-49-0 Structure
  • Basic information

    1. Product Name: 5-(1-adamantyl)-2-(4-methoxyphenyl)-1H-isoindole-1,3(2H)-dione
    2. Synonyms: 5-(1-adamantyl)-2-(4-methoxyphenyl)-1H-isoindole-1,3(2H)-dione
    3. CAS NO:303114-49-0
    4. Molecular Formula: C25H25NO3
    5. Molecular Weight: 387.4709
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 303114-49-0.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-(1-adamantyl)-2-(4-methoxyphenyl)-1H-isoindole-1,3(2H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(1-adamantyl)-2-(4-methoxyphenyl)-1H-isoindole-1,3(2H)-dione(303114-49-0)
    11. EPA Substance Registry System: 5-(1-adamantyl)-2-(4-methoxyphenyl)-1H-isoindole-1,3(2H)-dione(303114-49-0)
  • 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: 303114-49-0(Hazardous Substances Data)

303114-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 303114-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,1,1 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 303114-49:
(8*3)+(7*0)+(6*3)+(5*1)+(4*1)+(3*4)+(2*4)+(1*9)=80
80 % 10 = 0
So 303114-49-0 is a valid CAS Registry Number.

303114-49-0Downstream Products

303114-49-0Relevant articles and documents

Synthesis of Adamantyl-substituted benzenedicarboxylic acids and their derivatives

Betnev,Obukhova,Betnev,Klyuev,Pronin

, p. 399 - 401 (2007/10/03)

A new procedure was developed for the synthesis of adamantyl benzene derivatives by alkylation of o-and m-xylenes with l-adamantyl bromide. Adamantyl-substituted benzenedicarboxylic acids were synthesized by catalytic liquid-phase oxidation of the corresp

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