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Home > Encyclopedia > DIBENZYL DIISOPROPYLPHOSPHORAMIDITE

DIBENZYL DIISOPROPYLPHOSPHORAMIDITE

DIBENZYL DIISOPROPYLPHOSPHORAMIDITE structure

DIBENZYL DIISOPROPYLPHOSPHORAMIDITE 

structure
  • CAS No:

    108549-23-1

  • Formula:

    C20H28NO2P

  • Chemical Name:

    DIBENZYL DIISOPROPYLPHOSPHORAMIDITE

  • Synonyms:

    DIBENZYL DIISOPROPYLPHOSPHORAMIDITE;DIBENZYLOXY(DIISOPROPYLAMINO)PHOSPHINE;DIBENZYL N,N-DIISOPROPYLPHOSPHORAMIDITE;DIBENZYL-N,N-DIISOPROPYLPHOSPHOROAMIDITE;LABOTEST-BB LT00451623;DIBENZYL N,N-DIISOPROPYLPHOSPHORAMIDITE, TECHNICAL GRADE, 90%;bis(benzyloxy)(diisopropylamino)phosphine;β-cyanoethyl-N,N,N',N'-tetraisopropylphosphorodiamidite

  • Categories:

    Biochemical Engineering  >  Nucleoside Drugs

Description

Clear Colourless Liquid

DIBENZYL DIISOPROPYLPHOSPHORAMIDITE Basic Attributes

345.42

345.185760

2017-001-1

DTXSID70148584

29319090

Characteristics

21.7

4.8

1.028 g/mL at 25 °C(lit.)

130 °C0.55 mm Hg(lit.)

158 °F

n 20/D 1.535(lit.)

Soluble in chloroform.

Store at 0°C

Safety Information

NONH for all modes of transport

3

36/37/38

26-36-37/39

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 47 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

bis(benzyloxy)(diisopropylamino)phosphine

DIBENZYL DIISOPROPYLPHOSPHORAMIDITE Use and Manufacturing

Methods of Manufacturing

Take compound 3-9, 42g (207.92mmo1) was placed in a 500mL round bottomed flask, was added 300mL of anhydrous tetrahydrofuran, 66mL (455.44mmol, 46g) of anhydrous triethylamine were dissolved with stirring. When the flask was placed in an ice-salt bath until the system temperature was lowered to 0 the right, under nitrogen was added dropwise over anhydrous benzyl alcohol 45mL (416.67mmol, 45g), was added dropwise maintaining temperature of the system is always near 0 , IH complete after the suspension was added dropwise to give a white solid containing the ice bath was removed to room temperature, stirring was continued at room temperature for 3h stirring was stopped to stand 10min, filtered off with suction, washed solid was tetrahydrofuran, the filtrate was collected, rotary evaporated to give tetrahydrofuran was no liquid column liquid chromatography to give an oil 54.0g, a yield of 75.3percent.

Uses

A versatile phosphitylating agent

Computed Properties

Molecular Weight:345.4
XLogP3:4.8
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:9
Exact Mass:345.18576613
Monoisotopic Mass:345.18576613
Topological Polar Surface Area:21.7
Heavy Atom Count:24
Complexity:296
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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