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2-cyanoethyl N,N,N’,N’-tetraisopropyl-phosphordiamidite

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2-cyanoethyl N,N,N’,N’-tetraisopropyl-phosphordiamidite – Names and Identifiers

Name2-cyanoethyl N,N,N’,N’-tetraisopropyl-phosphordiamidite
Synonyms2-cyanoethyltetraisopropylphosphorodiamidite
2-Cyanoethyl N,N,N,N-tetraisopropylphosphorodiamitide
2-cyanoethyl N,N,N’,N’-tetraisopropyl-phosphordiamidite
2-Cyanoethyl N,N,N’,N’-tetraisopropylphosphorodiamidite
2-cyanoethyl N,N,N’,N’-tetrapropan-2-ylphosphorodiamidoite
P-(2-cyanoethyl)-N,N,N’,N’-tetrapropan-2-ylphosphonous diamide
CAS102691-36-1
EINECS600-337-9
InChIInChI=1/C15H32N3P/c1-12(2)17(13(3)4)19(11-9-10-16)18(14(5)6)15(7)8/h12-15H,9,11H2,1-8H3
InChIKeyRKVHNYJPIXOHRW-UHFFFAOYSA-N

2-cyanoethyl N,N,N’,N’-tetraisopropyl-phosphordiamidite – Physico-chemical Properties

Molecular FormulaC15H32N3P
Molar Mass285.408
Density0.949 g/mL at 25 °C(lit.)
Boling Point365.713°C at 760 mmHg
Flash Point174.977°C
Vapor Presure0mmHg at 25°C
Appearanceliquid
Colorcolorless
BRN3590103
pKa6.78±0.70(Predicted)
Storage Condition-20°C
StabilityExplodes When Heated
Sensitivemoisture sensitive, store cold
Refractive Indexn20/D 1.470(lit.)
UseBis (diisopropylamino) (2-cyanoethoxy) phosphine is an important reagent for the synthesis of oligonucleotides and antisense drugs. At present, there are two methods for the synthesis of bis (diisopropylamino) (2-cyanoethoxy) phosphine: Studies have disclosed a method for preparing bis (diisopropylamino) (2-cyanoethoxy) phosphine. The method is to react dichloro (2-cyanoethoxy) phosphine with diisopropylamine for 48-72 hours to obtain bis (diisopropylamino) (2-cyanoethoxy) phosphine, the main disadvantage of this method is that the raw material dichloro (2-cyanoethoxy) phosphine is an acid chloride, which is unstable, easy to deteriorate, has a long reaction time, and is difficult to purchase, so it is not conducive to industrial production. Another method for preparing bis (diisopropylamino) (2-cyanoethoxy) phosphine is to react bis (diisopropylamino) phosphine with 3-hydroxypropiononitrile for 20 hours to obtain bis (diisopropylamino) (2-cyanoethoxy) phosphine.

2-cyanoethyl N,N,N’,N’-tetraisopropyl-phosphordiamidite – Risk and Safety

Hazard SymbolsXi – Irritant

Risk CodesR5 – Heating may cause an explosion
R36/37/38 – Irritating to eyes, respiratory system and skin.
Safety DescriptionS3 – Keep in a cool place.
S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 – Wear suitable protective clothing.
UN IDsUN 1993
WGK Germany3
FLUKA BRAND F CODES10-21-34
HS Code29299000
Hazard NoteIrritant/May Explode on Heating
Hazard Class8
Packing GroupI

2-cyanoethyl N,N,N’,N’-tetraisopropyl-phosphordiamidite – Introduction

Application Bis (diisopropylamino) (2-cyanoethoxy) phosphine is an intermediate in organic synthesis and pharmaceutical research and development. It can be used to synthesize phosphite during laboratory research Reagents.
Preparation Add 15g tris (diisopropylamino) phosphine and 200ml dichloromethane to the three-mouth bottle, stir until completely dissolved, then add 3.86g of 3-hydroxypropiononitrile and 3.80g of 1H-tetrazole, and maintain the obtained solution at a temperature of -20 ° C- 0°C for reaction for 10 hours; Then, suction filtration and desalting, saturated sodium bicarbonate washing, saturated sodium chloride washing, liquid separation, sodium sulfate drying organic phase, suction filtration, the solvent is distilled under reduced pressure to obtain a white or light yellow liquid; the oil pump distilled under reduced pressure to obtain a colorless transparent liquid bis (diisopropylamino) (2-cyanoethoxy) phosphine 7g. 51.5% molar yield.
Reagents for the synthesis of phosphorite nucleotides

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Declaration: The products displayed on this website are intended exclusively for industrial applications or scientific research. They are not intended for medical, pharmaceutical, or food use. In accordance with applicable laws and regulations, purchasing organizations must hold valid qualifications and approvals.

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