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CAS

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69265-22-1

1-methyl-5-(1-methyl-ureido)-1H-imidazole-4-carboxylic acid amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69265-22-1 Structure

  • Basic information

    1. Product Name: 1-methyl-5-(1-methyl-ureido)-1H-imidazole-4-carboxylic acid amide
    2. Synonyms: 1-methyl-5-(1-methyl-ureido)-1H-imidazole-4-carboxylic acid amide
    3. CAS NO:69265-22-1
    4. Molecular Formula:
    5. Molecular Weight: 197.197
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69265-22-1.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: 1-methyl-5-(1-methyl-ureido)-1H-imidazole-4-carboxylic acid amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-methyl-5-(1-methyl-ureido)-1H-imidazole-4-carboxylic acid amide(69265-22-1)
    11. EPA Substance Registry System: 1-methyl-5-(1-methyl-ureido)-1H-imidazole-4-carboxylic acid amide(69265-22-1)

  • 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: 69265-22-1(Hazardous Substances Data)

69265-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69265-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,6 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69265-22:
(7*6)+(6*9)+(5*2)+(4*6)+(3*5)+(2*2)+(1*2)=151
151 % 10 = 1
So 69265-22-1 is a valid CAS Registry Number.

69265-22-1Upstream product

69265-22-1Downstream Products

69265-22-1Relevant articles and documents

SYNTHESIS OF 3,9-DIALKYLGUANINES AND THEIR CONVERSION INTO 3-ALKYLWYES, MODELS FOR THE FLUORESCENT NUCLEOSIDES FROM PHENYLALANINE TRANSFER RIBONUCLEIC ACIDS

Itaya, Taisuke,Ogawa, Kazuo

, p. 1767 - 1774 (1982)

Synthesis of 3,9-dialkylguanines 5 has been accomplished by N-cyanation of 1-alkyl-5-(alkylamino)imidazole-4-carboxamides 3 followed by base-catalysed cyclisation.Cyclocondensation of 9-alkyl-3-methylguanines 5a, d, f with MeCOCH2Br gave 3-alkylwyes 6, model compounds of the most probable structure for wyosine from Torulopsis utilis tRNAPhe.

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