ChemicalBook--->CAS DataBase List--->1309573-60-1

1309573-60-1

1309573-60-1 Structure

1309573-60-1 Structure
IdentificationBack Directory
[Name]

Poly(oxy-1,2-ethanediyl),α-[4-[[3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl]oxy]-1,4-dioxobutyl]-ω-methoxy-Polymer
[CAS]

1309573-60-1
[Synonyms]

TPGS-750-M
wt. % in H2O
DL-α-Tocopherol methoxypolyethylene glycol succinate
DL-alpha-Tocopherol methoxypolyethylene glycol succinate
DL-α-Tocopherol methoxypolyethylene glycol succinate solution
DL-alpha-Tocopherol methoxypolyethylene glycol succinate solution
DL-α-Tocopherol methoxypolyethylene glycol succinate solution 2 wt. % in H2O
DL-alpha-Tocopherol methoxypolyethylene glycol succinate solution (TPGS-750-M)
DL-alpha-Tocopherol Methoxypolyethylene glycol succinate solution 2 wt. % in H2O
Poly(oxy-1,2-ethanediyl),α-[4-[[3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl]oxy]-1,4-dioxobutyl]-ω-methoxy-Polymer
Poly(oxy-1,2-ethanediyl),α-[4-[[3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl]oxy]-1,4-dioxobutyl]-ω-methoxy-Polymer
[Molecular Formula]

(C2H4O)nC34H56O5
[MOL File]

1309573-60-1.mol
Chemical PropertiesBack Directory
[density ]

0.981 g/mL at 25 °C
[refractive index ]

n20/D1.340
[Fp ]

>110℃
[storage temp. ]

Store at -20°C
[form ]

Liquid
[color ]

Colorless to light yellow
[Water Solubility ]

Water: ≥ 50 mg/mL
Safety DataBack Directory
[WGK Germany ]

2
Hazard InformationBack Directory
[Uses]

DL-α-Tocopherol methoxypolyethylene glycol succinate (TPGS-750-M), a biodegradable and water-soluble derivative of natural vitamin E, is used as an environmentally benign nonionic surfactant in metal-catalyzed cross-coupling reactions in water. It is used in Heck, Suzuki-Miyaura, Sonogashira, and Negishi like couplings reactions. It can also be utilized in aminations, C-H activations, and olefin metathesis reactions.
TPGS-750-M can also be employed in:
  • The nucleophilic aromatic substitution reaction of aryl and heteroaryl halides with nitrogen, oxygen, and sulfur nucleophiles under mild conditions.
  • The preparation of quinoxaline-2,3 diones from quinoxalinones via C(sp2)-H hydroxylation reaction.
  • The intramolecular N-arylation of amines using a copper catalyst.

[Uses]

Second generation amphiphile which forms micelles upon dissolution in water allowing a variety of cross-coupling reactions to take place in water instead of organic solvent.

Included among the possible reactions are:
  • Olefin metathesis
  • Pd-catalyzed cross coupling reactions including Heck, Suzuki-Miyaura, Sonogashira and Buchwald-Hartwig reactions
  • C-H activation reactions

Second generation amphiphile for cross-coupling reactions in water
[General Description]

This product TPGS-750-M is a lead surfactant for many transition metal-catalyzed cross-couplings and has been enhanced for catalytic efficiency.
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