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153920-20-8

Adenosine, 5'-S-(4-chlorophenyl)-5'-thio- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153920-20-8 Structure

  • Basic information

    1. Product Name: Adenosine, 5'-S-(4-chlorophenyl)-5'-thio-
    2. Synonyms:
    3. CAS NO:153920-20-8
    4. Molecular Formula: C16H16ClN5O3S
    5. Molecular Weight: 393.854
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153920-20-8.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, 5'-S-(4-chlorophenyl)-5'-thio-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Adenosine, 5'-S-(4-chlorophenyl)-5'-thio-(153920-20-8)
    11. EPA Substance Registry System: Adenosine, 5'-S-(4-chlorophenyl)-5'-thio-(153920-20-8)

  • 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: 153920-20-8(Hazardous Substances Data)

153920-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153920-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,9,2 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153920-20:
(8*1)+(7*5)+(6*3)+(5*9)+(4*2)+(3*0)+(2*2)+(1*0)=118
118 % 10 = 8
So 153920-20-8 is a valid CAS Registry Number.

153920-20-8Relevant articles and documents

Nucleic acid related compounds. 80. Synthesis of 5'-S-(alkyl and aryl)-5'-fluoro-5'-thioadenosines with Xenon difluoride or (diethylamido)sulfur trifluoride, hydrolysis in aqueous buffer, and inhibition of S-adenosyl-L-homocysteine hydrolase by derived 'a

Robins,Wnuk,Mullah,Dalley,Yuan,Lee,Borchardt

, p. 544 - 555 (1994)

Treatment of 5'-S-(alkyl and aryl)-5'-thioadenosine derivatives 2 with XeF2, or the corresponding sulfoxides 3 with DAST/SbCl3, gave diastereomeric 5'-fluoro compounds which were deprotected to give the 5'-S-(alkyl and aryl)-5'-fluor

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