tris(1,1,1,3,3,3-hexafluoro-2-propyl) phosphite

tris(1,1,1,3,3,3-hexafluoro-2-propyl) phosphite Structure
tris(1,1,1,3,3,3-hexafluoro-2-propyl) phosphite structure
Common Name tris(1,1,1,3,3,3-hexafluoro-2-propyl) phosphite
CAS Number 66470-81-3 Molecular Weight 532.06300
Density 1.69 g/mL at 25ºC(lit.) Boiling Point 130ºC(lit.)
Molecular Formula C9H3F18O3P Melting Point N/A
MSDS Chinese USA Flash Point 44.5ºC
Symbol GHS07
GHS07
Signal Word Warning

Solid phase synthesis of oligoribonucleotides using the 1-[(2-chloro-4-methyl)phenyl]-4-methoxypiperidin-4-yl (Ctmp) group for the protection of the 2'-hydroxy functions and the H-phosphonate approach.

Nucleic Acids Res. 17(10) , 3689-97, (1989)

The solid phase synthesis of oligoribonucleotides using the H-phosphonate approach and the 1-[(2-chloro-4-methyl)phenyl]-4-methoxypiperidin-4-yl (Ctmp) and dimethoxytrityl (DMTr) groups, respectively, for the protection of the 2'- and 5'-hydroxy functions is ...

Use of new phosphonylating and coupling agents in the synthesis of oligodeoxyribonucleotides via the H-phosphonate approach.

Nucleic Acids Res. 18(11) , 3327-31, (1990)

New phosphonylating and coupling agents for the synthesis of oligodeoxyribonucleotides via H-phosphonate approach have been developed. Tris(1,1,1,3,3,3-hexafluoro-2-propyl) phosphite, prepared by the reaction of lithium salt of 1,1,1,3,3,3-hexafluoro-2-propox...

Stereoselective propargylation mediated by a chiral metal cluster: reactions of [(propargylium)Co2 (CO)5{P(OR)3}][BF4] with carbon nucleophiles. Caffyn AJM and Nicholas KM.

J. Am. Chem. Soc. 115(14) , 6438-6439, (1993)

Synthesis of antisense oligodeoxyribonucleotide analogues by use of deoxyribonucleoside 3'-bis(1,1, 1,3,3,3-hexafluoro-2-propyl)phosphites as new key intermediates. Hosaka H, et al.

Heteroatom Chem. 2(1) , 197-204, (1991)

Preparation and nuclear magnetic resonance studies of pentacoordinated phosphorus compounds containing hexafluoroisopropoxy groups. Denney DB, et al.

J. Org. Chem. 48(13) , 2159-2164, (1983)