Welcome to LookChem.com Sign In|Join Free

CAS

  • or

138870-21-0

N6-benzoyl-9-(RS)-(3-fluoro-2-hydroxypropyl)adenine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138870-21-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 138870-21-0 Structure

  • Basic information

    1. Product Name: N6-benzoyl-9-(RS)-(3-fluoro-2-hydroxypropyl)adenine
    2. Synonyms:
    3. CAS NO:138870-21-0
    4. Molecular Formula:
    5. Molecular Weight: 315.307
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138870-21-0.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: N6-benzoyl-9-(RS)-(3-fluoro-2-hydroxypropyl)adenine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N6-benzoyl-9-(RS)-(3-fluoro-2-hydroxypropyl)adenine(138870-21-0)
    11. EPA Substance Registry System: N6-benzoyl-9-(RS)-(3-fluoro-2-hydroxypropyl)adenine(138870-21-0)

  • 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: 138870-21-0(Hazardous Substances Data)

138870-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138870-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,8,7 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138870-21:
(8*1)+(7*3)+(6*8)+(5*8)+(4*7)+(3*0)+(2*2)+(1*1)=150
150 % 10 = 0
So 138870-21-0 is a valid CAS Registry Number.

138870-21-0Relevant articles and documents

SYNTHESIS OF N-(3-FLUORO-2-PHOSPHONOMETHOXYPROPYL) (FPMP) DERIVATIVES OF HETEROCYCLIC BASES

Jindrich, Jindrich,Holy, Antonin,Dvorakova, Hana

, p. 1645 - 1667 (2007/10/02)

A new groupnof compounds has been prepared: N-(3-fluoro-2-phosphonomethoxypropyl) (FPMP) derivatives of purine and pyrimidine bases which exhibit a significant selective activity against a broad spectrum of retroviruses.Racemic N-(3-fluoro-2-phosphonomethoxypropyl) derivatives of adenine (V), guanine (IX), cytosine (XIII), 2,6-diaminopurine (XXI), 3-deazaadenine (XVII), xanthine (X) and hypoxanthine (VI) were prepared from the corresponding n-(3-fluoro-2-hydroxypropyl) derivatives after protection of amino group at the heterocyclic ring by selective benzoylation, reaction with diisopropyl p-toluenesulfonyloxymethylphosphonate (II), and subsequent removal of the protecting groups.Chiral FPMP derivatives were prepared by reaction of heterocyclic base with corresponding chiral synthon (XXX; XXXVII) followed by deprotection.The required chiral synthons were obtained from enantiomeric 3-fluoro-1,2-propanediols by two methods.In the first, the primary hydroxyl group was tritylated, the obtained derivative was reacted with compound II, the trityl group was removed and the product was mesylated to give synthon XXXVII.The second pathway considered tosylation of the primary hydroxyl group and conversion of the secondary hydroxyl into the acetoxymethyl ether via the methoxymethyl ether; treatment of the acetoxy compound with bromotrimethylsilane and triisopropyl phosphite afforded the desired synthon XXX.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 138870-21-0