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122069-05-0

<(Difurfurylcarbamoyl)methyl>triphenylphosphoniumbromid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122069-05-0 Structure

  • Basic information

    1. Product Name: <(Difurfurylcarbamoyl)methyl>triphenylphosphoniumbromid
    2. Synonyms:
    3. CAS NO:122069-05-0
    4. Molecular Formula:
    5. Molecular Weight: 560.427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122069-05-0.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: <(Difurfurylcarbamoyl)methyl>triphenylphosphoniumbromid(CAS DataBase Reference)
    10. NIST Chemistry Reference: <(Difurfurylcarbamoyl)methyl>triphenylphosphoniumbromid(122069-05-0)
    11. EPA Substance Registry System: <(Difurfurylcarbamoyl)methyl>triphenylphosphoniumbromid(122069-05-0)

  • 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: 122069-05-0(Hazardous Substances Data)

122069-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122069-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122069-05:
(8*1)+(7*2)+(6*2)+(5*0)+(4*6)+(3*9)+(2*0)+(1*5)=90
90 % 10 = 0
So 122069-05-0 is a valid CAS Registry Number.

122069-05-0Relevant articles and documents

Cycloadditions, 17. - Influence of Methyl and Phenyl Groups in the Allenic ω-Position on the Thermally Induced Isomerizations of N-allenecarboxamides

Schlindwein, Hans-Juergen,Himbert, Gerhard

, p. 2331 - 2340 (2007/10/02)

The N-(2-hetarylmethyl)-1,2-alkadienecarboxamides 9a-q were synthesized by the ylide route, and their readiness to participate in the intramolecular Diels-Alder reaction was studied.Whereas the pyrrole derivatives 9p and 9q and the thiophene derivative 9o without directly bonded phenyl nuclei only decompose, the thiophene allenes 9m and 9n form the "normal" tricycles 12a and 12b by reaction of their amide phenyl nucleus (R1 = Ph).In all N-furfurylallenecarboxamides 9a-l the furan nucleus is involved in the intramolecular Diels-Alder reaction, irrespective of the amine substituent R1.The furan nucleus reacts in all cases with the terminal allenic double bond to form the oxatricycles 10a-l containing a six-membered lactam moiety.Reaction with the first allenic double bond (formation of 11c,d, and g) only takes place, when the reaction with the other double bond is slowed down by one or two methyl groups in the ω-position and the formation of 11 is not prevented by a methyl group in the furan 5-position. - Key Words: Diels-Alder reactions, intramolecular / Allenecarboxamides, N-(hetarylmethyl)-

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