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112404-30-5

2-(2-(4-BROMOPHENYL)-2-OXOETHYL)-2,5,5-TRIMETHYLCYCLOHEXANE-1,3-DIONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112404-30-5 Structure

  • Basic information

    1. Product Name: 2-(2-(4-BROMOPHENYL)-2-OXOETHYL)-2,5,5-TRIMETHYLCYCLOHEXANE-1,3-DIONE
    2. Synonyms: 2-(2-(4-BROMOPHENYL)-2-OXOETHYL)-2,5,5-TRIMETHYLCYCLOHEXANE-1,3-DIONE
    3. CAS NO:112404-30-5
    4. Molecular Formula: C17H19BrO3
    5. Molecular Weight: 351.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112404-30-5.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: 2-(2-(4-BROMOPHENYL)-2-OXOETHYL)-2,5,5-TRIMETHYLCYCLOHEXANE-1,3-DIONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-(4-BROMOPHENYL)-2-OXOETHYL)-2,5,5-TRIMETHYLCYCLOHEXANE-1,3-DIONE(112404-30-5)
    11. EPA Substance Registry System: 2-(2-(4-BROMOPHENYL)-2-OXOETHYL)-2,5,5-TRIMETHYLCYCLOHEXANE-1,3-DIONE(112404-30-5)

  • 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: 112404-30-5(Hazardous Substances Data)

112404-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112404-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,0 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112404-30:
(8*1)+(7*1)+(6*2)+(5*4)+(4*0)+(3*4)+(2*3)+(1*0)=65
65 % 10 = 5
So 112404-30-5 is a valid CAS Registry Number.

112404-30-5Relevant articles and documents

THE SYNTHESIS AND CHEMISTRY OF AZOLENINES. PART 8. THE PAAL-KNORR REACTION WITH CYCLIC 2-(ACYLMETHYL)-2-ALKYL-1,3-DIKETONES: ISOLATION OF 1-ACYL-1H-PYRROLES VIA REARRANGEMENT

Maini, Prem Nath,Sammes, Michael P.,Katritzky, Alan R.

, p. 161 - 168 (2007/10/02)

Treatment of cyclic 2-acylmethyl-2-alkyl-1,3-diketones with ammonium acetate under reflux in acetic acid gives moderate to high yields of 1-acyl-1H-pyrroles by rearrangement.Some of the cyclic diketones react quantitatively with liquid ammonia to yield 2-

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