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82829-07-0

5-iodofurfural dimorpholylaminal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82829-07-0 Structure

  • Basic information

    1. Product Name: 5-iodofurfural dimorpholylaminal
    2. Synonyms: 5-iodofurfural dimorpholylaminal
    3. CAS NO:82829-07-0
    4. Molecular Formula:
    5. Molecular Weight: 378.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82829-07-0.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: 5-iodofurfural dimorpholylaminal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-iodofurfural dimorpholylaminal(82829-07-0)
    11. EPA Substance Registry System: 5-iodofurfural dimorpholylaminal(82829-07-0)

  • 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: 82829-07-0(Hazardous Substances Data)

82829-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82829-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,2 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82829-07:
(7*8)+(6*2)+(5*8)+(4*2)+(3*9)+(2*0)+(1*7)=150
150 % 10 = 0
So 82829-07-0 is a valid CAS Registry Number.

82829-07-0Relevant articles and documents

Mechanism of the Reaction of Aldehydes of the Furan Series with Secondary Amines in Methanol

Novikov, V. N.,Borodaev, S. V.,Babeshkina, L. D.

, p. 448 - 454 (1982)

The reaction of 5-halofurfurals with piperidine and morpholine in methanol under various reaction conditions was investigated by means of spectrophotometry.The kinetics of the stepwise addition of the amine to the aldehyde function of the halofurfural were studied in the case of a dilute solution, while the conversion of the aldehyde to a 5-N,N-dialkylaminofurfurylidene-N,N-dialkylimmonium salt, for which two autocatalysis mechanisms were observed, was investigated in the case of a concentrated solution.Reaction intermediates, viz., 5-halofurfurylidene-N,N-bis(dialkylamines), were isolated preparatively and investigated.

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