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76837-69-9

6-(3-Hydroxy-N-methyl-anilino)-3-methyl-2,4(1H,3H)-pyrimidindion is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76837-69-9 Structure

  • Basic information

    1. Product Name: 6-(3-Hydroxy-N-methyl-anilino)-3-methyl-2,4(1H,3H)-pyrimidindion
    2. Synonyms:
    3. CAS NO:76837-69-9
    4. Molecular Formula:
    5. Molecular Weight: 247.254
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76837-69-9.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: 6-(3-Hydroxy-N-methyl-anilino)-3-methyl-2,4(1H,3H)-pyrimidindion(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(3-Hydroxy-N-methyl-anilino)-3-methyl-2,4(1H,3H)-pyrimidindion(76837-69-9)
    11. EPA Substance Registry System: 6-(3-Hydroxy-N-methyl-anilino)-3-methyl-2,4(1H,3H)-pyrimidindion(76837-69-9)

  • 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: 76837-69-9(Hazardous Substances Data)

76837-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76837-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,3 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76837-69:
(7*7)+(6*6)+(5*8)+(4*3)+(3*7)+(2*6)+(1*9)=179
179 % 10 = 9
So 76837-69-9 is a valid CAS Registry Number.

76837-69-9Relevant articles and documents

Donator-substituted 5-Deazaflavins, II: Hydroxy- and 8-Dimethylamino-5-deazaflavins - Model Compounds of Naturally Occuring (Deaza-)Flavocoenzyms

Grauert, Rolf W.

, p. 937 - 950 (2007/10/02)

Donator-substituted 5-deazaflavins 7 were prepared by a Vilsmeier procedure from the anilinouracil derivatives 5 via 6 as stable intermediates.Spectroscopic comparison of the 5-deazaflavins 7 shows, that resonance of the substituents increases in the sequ

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