Date published: 2026-4-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

Diallyl N,N-diisopropylphosphoramidite (CAS 126429-21-8)

0.0(0)
Write a reviewAsk a question

CAS Number:
126429-21-8
Purity:
≥90%
Molecular Weight:
245.30
Molecular Formula:
C12H24NO2P
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Diallyl N,N-diisopropylphosphoramidite is a reagent in the synthesis of Leustroducsin B and the synthesis of water-soluble prodrugs of triazole CS-758. Diallyl N,N-diisopropylphosphoramidite is an organophosphorus compound. This colorless liquid with a pungent odor serves as a precursor to phosphoramidites and phosphoramidates. It finds utility as a reagent in synthesizing a range of organic compounds, including peptidomimetics, peptides, and other molecules.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences


Diallyl N,N-diisopropylphosphoramidite (CAS 126429-21-8) References

  1. Syntheses of glucose derivatives of E5564-related compounds and their LPS-antagonistic activities.  |  Shiozaki, M., et al. 2006. Carbohydr Res. 341: 811-22. PMID: 16530740
  2. Synthesis and evaluation of a phosphonate analogue of the soluble guanylate cyclase activator YC-1.  |  Martin, NI., et al. 2007. Bioorg Med Chem Lett. 17: 4938-41. PMID: 17587571
  3. A highly convergent synthesis of myristoyl-carba(dethia)-coenzyme A.  |  Tautz, L. and Rétey, J. 2010. European J Org Chem. 2010: 1728-1735. PMID: 22347809
  4. Red-emitting rhodamines with hydroxylated, sulfonated, and phosphorylated dye residues and their use in fluorescence nanoscopy.  |  Kolmakov, K., et al. 2012. Chemistry. 18: 12986-98. PMID: 22968960
  5. A visualizable chain-terminating inhibitor of glycosaminoglycan biosynthesis in developing zebrafish.  |  Beahm, BJ., et al. 2014. Angew Chem Int Ed Engl. 53: 3347-52. PMID: 24554559
  6. Synthesis and SAR studies of benzyl ether derivatives as potent orally active S1P₁ agonists.  |  Tsuji, T., et al. 2014. Bioorg Med Chem. 22: 4246-56. PMID: 24909680
  7. Chemical synthesis of Burkholderia Lipid A modified with glycosyl phosphodiester-linked 4-amino-4-deoxy-β-L-arabinose and its immunomodulatory potential.  |  Hollaus, R., et al. 2015. Chemistry. 21: 4102-14. PMID: 25630448
  8. Xylosyltransferase II is the predominant isoenzyme which is responsible for the steady-state level of xylosyltransferase activity in human serum.  |  Kuhn, J., et al. 2015. Biochem Biophys Res Commun. 459: 469-74. PMID: 25748573
  9. Getting a grip on glycans: A current overview of the metabolic oligosaccharide engineering toolbox.  |  Sminia, TJ., et al. 2016. Carbohydr Res. 435: 121-141. PMID: 27750120
  10. Solid-Phase Modular Synthesis of Park Nucleotide and Lipids I and II Analogues.  |  Katsuyama, A., et al. 2018. Chem Pharm Bull (Tokyo). 66: 84-95. PMID: 29311516
  11. Total Synthesis and Structural Validation of Phosdiecin A via Asymmetric Alcohol-Mediated Carbonyl Reductive Coupling.  |  Della-Felice, F., et al. 2019. J Am Chem Soc. 141: 13778-13782. PMID: 31433167
  12. ArnD is a deformylase involved in polymyxin resistance.  |  Adak, T., et al. 2020. Chem Commun (Camb). 56: 6830-6833. PMID: 32432293
  13. Use of Allylic Protecting Groups for the Synthesis of Base-Sensitive Prooligonucleotides  |   and Nicolas Spinelli, Albert Meyer, Yoshihiro Hayakawa, Jean-Louis Imbach, Jean-Jacques Vasseur. January 2002. EurJOC (European Journal of Organic Chemistry). Volume2002, Issue1: Pages 49-56.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Diallyl N,N-diisopropylphosphoramidite, 1 g

sc-227766
1 g
$292.00