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Merck
CN

419362

Di-tert-butyl N,N-diisopropylphosphoramidite

95%, liquid

Synonym(s):

Di-tert-butyl diisopropylphosphoramidite

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About This Item

Linear Formula:
[(CH3)2CH]2NP[OC(CH3)3]2
CAS Number:
Molecular Weight:
277.38
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352001
MDL number:
Beilstein/REAXYS Number:
4858847
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Product Name

Di-tert-butyl N,N-diisopropylphosphoramidite, 95%

Quality Level

assay

95%

form

liquid

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: ligand

refractive index

n20/D 1.444 (lit.)

bp

85-90 °C/0.2 mmHg (lit.)

density

0.879 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC(C)N(C(C)C)P(OC(C)(C)C)OC(C)(C)C

InChI

1S/C14H32NO2P/c1-11(2)15(12(3)4)18(16-13(5,6)7)17-14(8,9)10/h11-12H,1-10H3

InChI key

YGFLCNPXEPDANQ-UHFFFAOYSA-N

Application

Di-tert-butyl N,N-diisopropylphosphoramidite is a general reagent to introduce tert-butyl-protected phosphate groups. It is commonly used in phosphorylation of biomolecules. It can also be used in the synthesis of phosphoramidate-linked glycoconjugates.


signalword

Warning

pictograms

Exclamation mark

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter



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Related Content

Phosphine Ligand Application Guide


Solid?Phase Synthesis of Phosphoramidate?Linked Glycopeptides.
Jaradat D S M, et al.
European Journal of Organic Chemistry, 2010(26), 5004-5009 (2010)
Synthesis, structure? activity relationships, and biological evaluation of fatty alcohol phosphates as lysophosphatidic acid receptor ligands, activators of PPARγ, and inhibitors of autotaxin.
Durgam G G, et al.
Journal of Medicinal Chemistry, 48(15), 4919-4930 (2005)
Fluorogenic peptide substrates for serine and threonine phosphatases.
Xue F and Seto C T
Organic Letters, 12(9), 1936-1939 (2010)



Global Trade Item Number

SKUGTIN
419362-1G04061838098092
419362-5G04061832092102