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223116-03-8

Adenosine, 3'-deoxy-3'-[[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-1-oxo-3-phen ylpropyl]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 223116-03-8 Structure

  • Basic information

    1. Product Name: Adenosine, 3'-deoxy-3'-[[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-1-oxo-3-phen ylpropyl]amino]-
    2. Synonyms:
    3. CAS NO:223116-03-8
    4. Molecular Formula: C24H31N7O6
    5. Molecular Weight: 513.553
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 223116-03-8.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: Adenosine, 3'-deoxy-3'-[[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-1-oxo-3-phen ylpropyl]amino]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Adenosine, 3'-deoxy-3'-[[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-1-oxo-3-phen ylpropyl]amino]-(223116-03-8)
    11. EPA Substance Registry System: Adenosine, 3'-deoxy-3'-[[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-1-oxo-3-phen ylpropyl]amino]-(223116-03-8)

  • 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: 223116-03-8(Hazardous Substances Data)

223116-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 223116-03-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,1,1 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 223116-03:
(8*2)+(7*2)+(6*3)+(5*1)+(4*1)+(3*6)+(2*0)+(1*3)=78
78 % 10 = 8
So 223116-03-8 is a valid CAS Registry Number.

223116-03-8Relevant articles and documents

Synthesis of pCpCpA-3′-NH-phenylalanine as a ribosomal substrate

Zhang, Biliang,Zhang, Lei,Sun, Lele,Cui, Zhiyong

, p. 3615 - 3618 (2002)

(equation presented) The trinucleotide cytidylyl(3′→5′phosphoryl)cytidylyl(3′- 5′phosphoryl)-3′-deoxy-3′-(L-phenylalanyl) amido adenosine (CpCpA-NH-Phe) was synthesized by phosphoramidite chemistry from 3′-amino-3′-deoxyadenosine as the ribosomal substrat

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