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220280-01-3

1H-Pyrrole,1-(1,1-dimethylethyl)-3,4-diethoxy-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 220280-01-3 Structure

  • Basic information

    1. Product Name: 1H-Pyrrole,1-(1,1-dimethylethyl)-3,4-diethoxy-(9CI)
    2. Synonyms: 1H-Pyrrole,1-(1,1-dimethylethyl)-3,4-diethoxy-(9CI)
    3. CAS NO:220280-01-3
    4. Molecular Formula: C12H21NO2
    5. Molecular Weight: 211.30064
    6. EINECS: N/A
    7. Product Categories: ETHOXY
    8. Mol File: 220280-01-3.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: 1H-Pyrrole,1-(1,1-dimethylethyl)-3,4-diethoxy-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrrole,1-(1,1-dimethylethyl)-3,4-diethoxy-(9CI)(220280-01-3)
    11. EPA Substance Registry System: 1H-Pyrrole,1-(1,1-dimethylethyl)-3,4-diethoxy-(9CI)(220280-01-3)

  • 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: 220280-01-3(Hazardous Substances Data)

220280-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220280-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,8 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 220280-01:
(8*2)+(7*2)+(6*0)+(5*2)+(4*8)+(3*0)+(2*0)+(1*1)=73
73 % 10 = 3
So 220280-01-3 is a valid CAS Registry Number.

220280-01-3Downstream Products

220280-01-3Relevant articles and documents

A short and efficient synthesis of 3,4-dialkoxypyrroles

Merz, Andreas,Meyer, Thomas

, p. 94 - 99 (2007/10/03)

3,4-Dialkoxypyrroles are obtained in four steps from commercially available 2,5-dimethoxy-2,5-dihydrofuran (1). The dihydrofuran 1 is first oxidized by KMnO4 to the diol 2 which is bis-alkylated to 3a-d. Reaction of the in situ generated dialdehydes with a primary amine affords the N- substituted dialkoxypyrroles 4a-m. N-Benzyl-3,4-dialkoxypyrroles and N- allyl-dialkoxypyrroles are cleaved by sodium in liquid ammonia affording N- unsubstituted dialkoxypyrroles 5a-c in good overall yield.

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