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130404-30-7

Benzenepropanamide, N-(6-amino-1,2,3,4-tetrahydro-2,4-dioxo-1,3-dipropyl-5-pyrimidinyl)-a- methyl-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130404-30-7 Structure

  • Basic information

    1. Product Name: Benzenepropanamide, N-(6-amino-1,2,3,4-tetrahydro-2,4-dioxo-1,3-dipropyl-5-pyrimidinyl)-a- methyl-, (R)-
    2. Synonyms:
    3. CAS NO:130404-30-7
    4. Molecular Formula: C20H28N4O3
    5. Molecular Weight: 372.467
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130404-30-7.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: Benzenepropanamide, N-(6-amino-1,2,3,4-tetrahydro-2,4-dioxo-1,3-dipropyl-5-pyrimidinyl)-a- methyl-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenepropanamide, N-(6-amino-1,2,3,4-tetrahydro-2,4-dioxo-1,3-dipropyl-5-pyrimidinyl)-a- methyl-, (R)-(130404-30-7)
    11. EPA Substance Registry System: Benzenepropanamide, N-(6-amino-1,2,3,4-tetrahydro-2,4-dioxo-1,3-dipropyl-5-pyrimidinyl)-a- methyl-, (R)-(130404-30-7)

  • 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: 130404-30-7(Hazardous Substances Data)

130404-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130404-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,0 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 130404-30:
(8*1)+(7*3)+(6*0)+(5*4)+(4*0)+(3*4)+(2*3)+(1*0)=67
67 % 10 = 7
So 130404-30-7 is a valid CAS Registry Number.

130404-30-7Relevant articles and documents

Xanthines with C8 chiral substituents as potent and selective adenosine A1 antagonists.

Peet,Lentz,Dudley,Ogden,McCarty,Racke

, p. 4015 - 4020 (2007/10/02)

Several 8-substituted 1,3-dipropylxanthines were synthesized, and their receptor binding affinities at adenosine A1 and A2 receptors were measured. When enantiomeric pairs of compounds were examined, the R enantiomers were significantly more potent than the corresponding S enantiomers. The most potent compound at the A1 receptor was (R)-3,7-dihydro-8-(1-methyl-2-phenylethyl)-1,3-dipropyl-1H-purine-2,6-di one (5a; MDL 102,503), whose Ki value at the A1 receptor was 6.9 nM. However, a more selective compound was (R)-3,7-dihydro-8-(1-phenylpropyl)-1,3-dipropyl-1H-purine-2,6-dione (5d; MDL 102,234), which had a Ki value of 23.2 nM at the A1 receptor and an A2/A1 ratio of 153.

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