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DIBENZYL DIISOPROPYLPHOSPHORAMIDITE

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CAS:108549-23-1
Purity:99%+ Package:100g;0.00;USD|250g;0.00;USD|500g;0.00;USD
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Products Intro: Product Name:Dibenzyl-N,N-disisopropylphosphoramidite
CAS:108549-23-1
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CAS:108549-23-1
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CAS:108549-23-1
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Products Intro: Product Name:Dibenzyl diisopropylphosphoramidite
CAS:108549-23-1
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg

DIBENZYL DIISOPROPYLPHOSPHORAMIDITE manufacturers

DIBENZYL DIISOPROPYLPHOSPHORAMIDITE Basic information
Product Name:DIBENZYL DIISOPROPYLPHOSPHORAMIDITE
Synonyms:N-[bis(phenylmethoxy)phosphanyl]-N-propan-2-yl-propan-2-amine;N-[bis(phenylmethoxy)phosphanyl]-N-propan-2-ylpropan-2-amine;Dibenzyl-N,N-disisopropylphosphoramidite;Dibenzyl N,N-diisopropylphosphoramidite, 95+%;Dibenzyl N,N-diisopropylphosphoramidite, tech 90%;DIBENZYL N,N-DIISOPRO;DIBENZYL DIISOPROPYLPHOSPHORAMIDITE;DIBENZYLOXY(DIISOPROPYLAMINO)PHOSPHINE
CAS:108549-23-1
MF:C20H28NO2P
MW:345.42
EINECS:629-628-9
Product Categories:OLED materials,pharm chemical,electronic;Organic Building Blocks;Phosphoramidites;Phosphorus Compounds;Phospholipids - 13C & 2H;Biochemistry;Nucleosides, Nucleotides & Related Reagents;Phosphorylating and Phosphorothioating Agents;Phosphorylation;Protecting Agents, Phosphorylating Agents & Condensing Agents;Synthetic Organic Chemistry;Phosphorylating and Phosphitylating Agents;SiChem;OLED
Mol File:108549-23-1.mol
DIBENZYL DIISOPROPYLPHOSPHORAMIDITE Structure
DIBENZYL DIISOPROPYLPHOSPHORAMIDITE Chemical Properties
Boiling point 130 °C0.55 mm Hg(lit.)
density 1.028 g/mL at 25 °C(lit.)
refractive index n20/D 1.535(lit.)
Fp 158 °F
storage temp. 2-8°C
solubility Soluble in chloroform.
pka4.50±0.70(Predicted)
form Oil
color Clear Colourless
Water Solubility THF: soluble(lit.)
acetonitrile: soluble(lit.)
cold water: insoluble(lit.)
dichloromethane: soluble(lit.)
Sensitive Moisture Sensitive
BRN 3616864
InChIInChI=1S/C20H28NO2P/c1-17(2)21(18(3)4)24(22-15-19-11-7-5-8-12-19)23-16-20-13-9-6-10-14-20/h5-14,17-18H,15-16H2,1-4H3
InChIKeyANPWLBTUUNFQIO-UHFFFAOYSA-N
SMILESP(N(C(C)C)C(C)C)(OCC1=CC=CC=C1)OCC1=CC=CC=C1
CAS DataBase Reference108549-23-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
3-10-21
HS Code 29319090
Storage Class10 - Combustible liquids
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
DIBENZYL DIISOPROPYLPHOSPHORAMIDITE Usage And Synthesis
DescriptionDibenzyl diisopropylphosphoramidite is a versatile phosphitylating agent.
Chemical PropertiesClear Colourless Liquid
UsesA versatile phosphitylating agent
UsesDibenzyl N,N-diisopropylphosphoramidite may be used for the preparation of phosphopeptides. It is used for the synthesis of a GDP (guanosine diphosphate) analog, SML-8-73-1. It is useful for nucleotide coupling.
Synthesis
DIISOPROPYLPHOSPHORAMIDOUS DICHLORIDE

921-26-6

Benzyl alcohol

100-51-6

DIBENZYL DIISOPROPYLPHOSPHORAMIDITE

108549-23-1

General procedure for the synthesis of diphenyl N,N'-diisopropylphosphoramidite from dichloro-N,N-diisopropylphosphoramidite and benzyl alcohol: 42 g (207.92 mmol) of dichloro-N,N-diisopropylphosphoramidite was placed in a 500 mL round-bottomed flask, and 300 mL of anhydrous tetrahydrofuran was added, and dissolved by stirring. Subsequently 66 mL (455.44 mmol, 46 g) of anhydrous triethylamine was added. The flask was cooled to 0°C in an ice-salt bath and 45 mL (416.67 mmol, 45 g) of anhydrous benzyl alcohol was added slowly and dropwise under nitrogen protection, keeping the reaction temperature close to 0°C. Upon completion of the reaction, the suspension was added dropwise and the formation of a white solid was observed. The reaction mixture was removed from the ice bath, returned to room temperature and stirring was continued for 3 hours. After stopping stirring, it was allowed to stand for 10 minutes for filtration and the solid was washed with tetrahydrofuran. The filtrate was collected and the solvent was removed by rotary evaporation to give the crude product. Without column chromatographic purification, 54.0 g of the oily product was obtained directly in 75.3% yield.

References[1] Tetrahedron, 1991, vol. 47, # 26, p. 4709 - 4722
[2] Patent: CN102977145, 2017, B. Location in patent: Paragraph 0196; 0197
[3] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1993, # 11, p. 1239 - 1246
[4] Journal of Medicinal Chemistry, 1994, vol. 37, # 23, p. 3918 - 3927
[5] Journal of Organic Chemistry, 1996, vol. 61, # 22, p. 7719 - 7726
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