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1H-Pyrrole-3-carboxaldehyde,1-(1,2-propadienyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104501-13-5 Structure
  • Basic information

    1. Product Name: 1H-Pyrrole-3-carboxaldehyde,1-(1,2-propadienyl)-(9CI)
    2. Synonyms: 1H-Pyrrole-3-carboxaldehyde,1-(1,2-propadienyl)-(9CI)
    3. CAS NO:104501-13-5
    4. Molecular Formula: C8H7NO
    5. Molecular Weight: 133.14728
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 104501-13-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 139.1±23.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.95±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -6.70±0.70(Predicted)
    10. CAS DataBase Reference: 1H-Pyrrole-3-carboxaldehyde,1-(1,2-propadienyl)-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Pyrrole-3-carboxaldehyde,1-(1,2-propadienyl)-(9CI)(104501-13-5)
    12. EPA Substance Registry System: 1H-Pyrrole-3-carboxaldehyde,1-(1,2-propadienyl)-(9CI)(104501-13-5)
  • 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: 104501-13-5(Hazardous Substances Data)

104501-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104501-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,0 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104501-13:
(8*1)+(7*0)+(6*4)+(5*5)+(4*0)+(3*1)+(2*1)+(1*3)=65
65 % 10 = 5
So 104501-13-5 is a valid CAS Registry Number.

104501-13-5Upstream product

104501-13-5Downstream Products

104501-13-5Relevant articles and documents

Novel pyrrole derivatives

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, (2008/06/13)

Novel pyrrole derivatives of the formula STR1 wherein one of R2 and R3 is STR2 and the other of R2 and R3 as well as R4 and R5 are individually selected from the group consisting of hydrogen, halogen, alkyl of 1 to 18 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 7 to 18 carbon atoms, --CN, --CF3, --NO2, --COOAlk and Alk is alkyl of 1 to 8 carbon atoms, alkoxy of 1 to 8 carbon atoms, STR3 n is 0, 1 or 2, R', R1 ' and R2 ' are alkyl of 1 to 8 carbon atoms and R4 and R5 taken together with the carbon atoms to which they are attached may form an optionally further unsaturated carbon homocycle of up to 8 carbon atoms, Z is selected from the group consisting of hydrogen, --CN, --C CH, --CF3 and alkyl of 1 to 3 carbon atoms, A is the residue of a pyrethrinoid acid, R1 is selected from the group consisting of STR4 X', X, Y, Y' and Y" are individually selected from the group consisting of hydrogen, halogen, alkyl of 1 to 8 carbon atoms and aryl of 6 to 14 carbon atoms, the dotted line indicating an optional double bond, r' is selected from the group consisting of hydrogen, alkyl of 1 to 18 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 7 to 18 carbon atoms, --CF3, --COOAlk and alkoxy of 1 to 8 carbon atoms and Alk has the above definition, R" and R'" are individually selected from the group consisting of hydrogen, alkyl of 1 to 8 carbon atoms, aryl of 6 to 14 carbon atoms, aralkyl of 6 to 18 carbon atoms, --CF3 ' --COOAlk' and alkoxy of 1 to 8 carbon atoms and Alk' is alkyl of 1 to 8 carbon atoms having pesticidal properties and novel intermediates.

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