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112088-82-1

9H-Purine, 9-[(3-bromophenyl)methyl]-6-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112088-82-1 Structure

  • Basic information

    1. Product Name: 9H-Purine, 9-[(3-bromophenyl)methyl]-6-chloro-
    2. Synonyms:
    3. CAS NO:112088-82-1
    4. Molecular Formula: C12H8BrClN4
    5. Molecular Weight: 323.579
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112088-82-1.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: 9H-Purine, 9-[(3-bromophenyl)methyl]-6-chloro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9H-Purine, 9-[(3-bromophenyl)methyl]-6-chloro-(112088-82-1)
    11. EPA Substance Registry System: 9H-Purine, 9-[(3-bromophenyl)methyl]-6-chloro-(112088-82-1)

  • 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: 112088-82-1(Hazardous Substances Data)

112088-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112088-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,8 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112088-82:
(8*1)+(7*1)+(6*2)+(5*0)+(4*8)+(3*8)+(2*8)+(1*2)=101
101 % 10 = 1
So 112088-82-1 is a valid CAS Registry Number.

112088-82-1Relevant articles and documents

6-(Alkylamino)-9-benzyl-9H-purines. A New Class of Anticonvulsant Agents

Kelley, James L.,Krochmal, Mark P.,Linn, James A.,McLean, Ed W.,Soroko, Francis E.

, p. 606 - 612 (2007/10/02)

Several 9-alkyl-6-substituted-purines were synthesized and tested for anticonvulsant activity against maximal electroshock-induced seizures (MES) in rats.Most compounds were prepared in three steps from 5-amino-4,6-dichloropyrimidine or in two steps via alkylation of 6-chloropurine.Potent anticonvulsant activity against MES resided in compounds that contain a benzyl substituent at the 9-position of 6-(methylamino)- or 6-(dimethylamino)purine.Among commonly used agents for control of seizures, this type of structure represents a new class of potent anticonvulsant agents.

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