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CS-W001157 4
Total: USD 88.00

4-Amino-5-iodopyrimidin-2(1H)-one

  • CAS No. 1122-44-7

  • Cat. No. CS-M0719
  • Purity≥98%
  • MDL No.MFCD00023162

*For research and further manufacturing use only, not for direct human use.

4-Amino-5-iodopyrimidin-2(1H)-one|CS-M0719

Structure of 1122-44-7

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General Information

  • CAS No. 1122-44-7
  • Cat. No. CS-M0719
  • Purity ≥98%
  • MDL No. MFCD00023162
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄H₄IN₃O
  • Molecular Weight 237.00
  • Synonym(s) 6-amino-5-iodopyrimidin-2(1H)-one
  • SMILES O=C1N=C(N)C(I)=CN1

Description

Grubbs Catalyst M204 can be used as a catalyst for ring-closing metathesis (RCM), cross-metathesis, and ring-opening metathesis polymerization (ROMP). It is also used to synthesize trisubstituted olefins with excellent functional group tolerance and selectivity via cross-metathesis and ring closing metathesis reactions.It can also be used as a catalyst:To synthesize coumarins from phenolic compounds via RCM.To cleave secondary (E)-allyl vic-diols to aldehydes.ChemBeads are chemical coated glass beads. ChemBeads offer improved flowability and chemical uniformity perfect for automated solid dispensing and high-throughput experimentation. The method of creating ChemBeads uses no other chemicals or surfactants allowing the user to accurately dispense sub-milligram amounts of chemical.Learn more about ChemBeads products For larger scale uses, product is also available in powdered form (569747)

Synthesis

  • Route1
    • Cytosine Lamivudine Impurity|CS-0214072
      71-30-7
    • ~99%
    • In-stock
      4-Amino-5-iodopyrimidin-2(1H)-one|CS-M0719
      1122-44-7

    References

    • Benner, Steven Albert Patent: US7741294 B1, 2010 ; Location in patent: Page/Page column 17 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P501

Quality Control

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Computational Chemistry Data

  • TPSA   71.77
  • LogP   -0.0433
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   0

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