tert-Butyl P, P - diméthylphosphonoacétate ,>=97,0% (GC)

Code: 79522-25ml D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Reactant for: Preparation of phosphonate terminated PPH dendrimers as anti-HIV-1 agents Preparation of monodehydro diketopiperazines from ketoacyl amino acid amid...


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Votre prix
$333.86 25ML

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Reactant for: Preparation of phosphonate terminated PPH dendrimers as anti-HIV-1 agents Preparation of monodehydro diketopiperazines from ketoacyl amino acid amides via acid-catalyzed cyclization Preparation of α,β-unsaturated esters for use in the guanidine-catalyzed oxa-Michael addition Preparation of myxopyronin B and desmethyl myxopyronin B analogs, with antibacterial activity and inhibitory activity against bacterial RNA polymerase Allylation and subsequent ring-closing metathesis in presence of Grubbs′ catalyst or intramolecular rhodium-catalyzed cyclopropanation reactions

Other Notes

Horner-Wittig reagent giving preferentially (E)-α,β-unsat. esters which are mildly saponified with acid. Synthesis of derivatives by reductive alkylation

Packaging

25, 100 mL in glass bottle

assay≥97.0% (GC)
bp86-87 °C/0.02 mmHg (lit.)
density1.131 g/mL at 20 °C (lit.)
formliquid
InChI keySAZYDWOWLRDDRQ-UHFFFAOYSA-N
InChI1S/C8H17O5P/c1-8(2,3)13-7(9)6-14(10,11-4)12-5/h6H2,1-5H3
Quality Level100
reaction suitabilityreaction type: C-C Bond Formation
refractive indexn20/D 1.434
SMILES stringCOP(=O)(CC(=O)OC(C)(C)C)OC
Cas Number62327-21-3
Ce produit répond aux critères suivants pour être admissible aux récompenses suivantes :



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