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Tetraethyl methylenediphosphonate, 98+%, Thermo Scientific Chemicals
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Catalog number A14532.14
also known as A14532-14
Price (USD)/ Each
272.65
Online exclusive
303.00 Save 30.35 (10%)
-
Quantity:
25 g
Price (USD)/ Each
272.65
Online exclusive
303.00 Save 30.35 (10%)
Tetraethyl methylenediphosphonate, 98+%, Thermo Scientific Chemicals
Catalog numberA14532.14
Price (USD)/ Each
272.65
Online exclusive
303.00 Save 30.35 (10%)
-
Chemical Identifiers
CAS1660-94-2
Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
Identification (FTIR)Conforms
Assay (GC)≥98.0%
FormLiquid
Refractive Index1.4405-1.4445 @ 20?C
Tetraethyl methylidenediphosphonate is used in the synthesis of tetrazoloquinoline-based mono- and bisphosphonate esters. It acts as an intermediate for the synthesis of bisphosphonate and bisphosphonic acid derivatives with anticancer and antischistosomal activity. It is also used as a reactant for synthesis of dual substrate-site inhibitors of 3-deoxy-D-arabino-heputosonate 7-phosphate synthase and alpha-amino acid derivatives containing gem-biophosphonates, Lycopene through Wittig-Horner reaction. It is also used as a precursor for the preparation of dendritic polyglycerol anions.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Tetraethyl methylidenediphosphonate is used in the synthesis of tetrazoloquinoline-based mono- and bisphosphonate esters. It acts as an intermediate for the synthesis of bisphosphonate and bisphosphonic acid derivatives with anticancer and antischistosomal activity. It is also used as a reactant for synthesis of dual substrate-site inhibitors of 3-deoxy-D-arabino-heputosonate 7-phosphate synthase and alpha-amino acid derivatives containing gem-biophosphonates, Lycopene through Wittig-Horner reaction. It is also used as a precursor for the preparation of dendritic polyglycerol anions.
Solubility
Slightly miscible with water.
Notes
Incompatible with strong oxidizing agents.
Tetraethyl methylidenediphosphonate is used in the synthesis of tetrazoloquinoline-based mono- and bisphosphonate esters. It acts as an intermediate for the synthesis of bisphosphonate and bisphosphonic acid derivatives with anticancer and antischistosomal activity. It is also used as a reactant for synthesis of dual substrate-site inhibitors of 3-deoxy-D-arabino-heputosonate 7-phosphate synthase and alpha-amino acid derivatives containing gem-biophosphonates, Lycopene through Wittig-Horner reaction. It is also used as a precursor for the preparation of dendritic polyglycerol anions.
Solubility
Slightly miscible with water.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Reacts with aromatic aldehydes to give styrylphosphonates in a two-phase system, no added phase-transfer catalyst being necessary: Synthesis, 396 (1976). For cleavage of the resulting vinyl phosphonates to ɑ-hydroxyaldehydes, see Osmium(VIII) oxide, 12103.
- Pachl, P.; Simak, O.; Rezacova, P.; Fabry, M.; Budesínsky, M.; Rosenberg, I.; Brynda, J. Structure-based design of a bisphosphonate 5'(3')-deoxyribonucleotidase inhibitor. Med. Chem. Commun. 2015, 6 (9), 1635-1638.
- Faísca Phillips, A. M.; Barros, M. T. Enantioselective Organocatalytic Synthesis of α-Cyclopropylphosphonates through a Domino Michael Addition/Intramolecular Alkylation Reaction. Eur. J. Org. Chem. 2014, 2014 (1), 152-163.