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methyl 3,5-di-O-(4-chlorobenzyl)-2-deoxy-2-fluoro-D-ribofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156357-11-8 Structure
  • Basic information

    1. Product Name: methyl 3,5-di-O-(4-chlorobenzyl)-2-deoxy-2-fluoro-D-ribofuranoside
    2. Synonyms:
    3. CAS NO:156357-11-8
    4. Molecular Formula:
    5. Molecular Weight: 415.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156357-11-8.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: methyl 3,5-di-O-(4-chlorobenzyl)-2-deoxy-2-fluoro-D-ribofuranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3,5-di-O-(4-chlorobenzyl)-2-deoxy-2-fluoro-D-ribofuranoside(156357-11-8)
    11. EPA Substance Registry System: methyl 3,5-di-O-(4-chlorobenzyl)-2-deoxy-2-fluoro-D-ribofuranoside(156357-11-8)
  • 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: 156357-11-8(Hazardous Substances Data)

156357-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156357-11-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,5 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 156357-11:
(8*1)+(7*5)+(6*6)+(5*3)+(4*5)+(3*7)+(2*1)+(1*1)=138
138 % 10 = 8
So 156357-11-8 is a valid CAS Registry Number.

156357-11-8Relevant articles and documents

Synthesis and biologic activity of purine 2'-deoxy-2'-fluoro- ribonucleosides

Thomas,Tiwari,Clayton,Secrist III,Montgomery

, p. 309 - 323 (2007/10/02)

The synthesis of 3,5-di-O-benzoyl-2-deoxy-2-fluoro-D-ribofuranosyl bromide (8) and its reaction with 2,6-dichloropurine by fusion and with mercuric cyanide catalysis is described. The resulting 2,6-dichloro-9-(3,5-di-O- benzoyl-2-deoxy-2-fluoro-β-D-ribofuranosyl)purine (13) was converted to the 2-fluoroadenine (16), the 2-chloroadenine (17), 2,6-diaminopurine (12), and guanine (14) nucleosides by standard procedures. These nucleosides were cytotoxic to a number of cell lines in culture. The 2-haloadenine nucleosides 16 and 17 gave modest increases in lifespan when tested against the P388 leukemia in mice.

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