Behenoyl-arabinofuranosyl-cytosine

Base Information

• Chemical Name: Behenoyl-arabinofuranosyl-cytosine
• CAS No.: 55726-47-1
• Molecular Formula: C₃₁H₅₅N₃O₆
• Molecular Weight: 565.794
• NSC Number: 239336
• DSSTox Substance ID: DTXSID00860686
• ChEMBL ID: CHEMBL1965199
• Mol file: 55726-47-1.mol

Synonyms:BEHENOYL-ARABINOFURANOSYL-CYTOSINE;N-[1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-oxopyrimidin-4-yl]docosanamide;BHAC;BH-AC;4-(docosanoylamino)-1-pentofuranosylpyrimidin-2(1h)-one;SCHEMBL7963;CHEMBL1965199;DTXSID00860686;DOCOSANAMIDE,NUCLEOSIDE DERIV;NSC239336;AKOS015895202;SB67389;NCGC00167964-01;NCI60_001919;FT-0630685;N4-BEHENOYL-1-B-D-ARABINOSYLCYTOSINE;Docosanamide,2-dihydro-2-oxo-4-pyrimidinyl)-

Chemical Property of Behenoyl-arabinofuranosyl-cytosine

Chemical Property:

• Melting Point: 141-142°C
• Refractive Index: 1.554
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 133.91000
• Density: 1.16g/cm³
• LogP: 5.68820
• Storage Temp.: -20°C Freezer
• Solubility.: DMSO (Slightly, Heated), Methanol (Slightly, Heated), THF (Slightly, Heated, Son
• XLogP3: 9.2
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 23
• Exact Mass: 565.40908648
• Heavy Atom Count: 40
• Complexity: 774

Purity/Quality:

97% ^*data from raw suppliers

Enocitabine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCC(=O)NC1=NC(=O)N(C=C1)C2C(C(C(O2)CO)O)O
• Description: Enocitabine is an antileukemic agent closely related to cytarabine. It appears more resistant to deamination than cytarabine, thus allowing greater in vivo phosphorylation into an active cytotoxic metabolite.
• Uses: An antineoplastic. A derivative of Cytarabine. An antineoplastic. A derivative of Cytarabine

Technology Process of Behenoyl-arabinofuranosyl-cytosine

There total 1 articles about Behenoyl-arabinofuranosyl-cytosine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.4%

→ N4-Behenoyl-1-β-D-arabinofuranosylcytosin (55726-47-1,93974-11-9)

Guidance literature:

Refernces

• 1、 -. "N4 -acylarabinonucleosides". . . Retrieved 2008/06/13.