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About This Item
Linear Formula:
[(CH3)2CH]2NP(Cl)OCH2CH2CN
CAS Number:
Molecular Weight:
236.68
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3588525
Form:
liquid
form
liquid
Quality Level
composition
Cl, 13.5-15.5%
refractive index
n/D 1.476-1.480
bp
103 -105 °C/0.1 hPa
density
1.061 g/mL at 25 °C (lit.)
functional group
amine, nitrile
storage temp.
−20°C
SMILES string
CC(C)N(C(C)C)P(Cl)OCCC#N
InChI
1S/C9H18ClN2OP/c1-8(2)12(9(3)4)14(10)13-7-5-6-11/h8-9H,5,7H2,1-4H3
InChI key
QWTBDIBOOIAZEF-UHFFFAOYSA-N
Application
2-Cyanoethyl N,N-diisopropylchlorophosphoramidite was employed:
- for selective monophosphorylation of carbohydrates and nucleosides
- for conversion of protected ribonucleosides to phosphoramidites
- as phosphitylating reagent for 3′-hydroxyl groups in the synthesis of oligodeoxyribonucleotides
- in a scalable, solution-phase oligonucleotide synthesis employing phosphoramidite chemistry and DMT-, iBu- and Bz-protected monomers. Intermediates were isolated by extraction without further purification
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Pyr. Liq. 1 - Skin Corr. 1B
Storage Class
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Organic Process Research & Development, 10, 1238-1238 (2006)
A Ono et al.
Bioconjugate chemistry, 4(6), 499-508 (1993-11-01)
Novel 2'-deoxyuridine analogues carrying aminoalkyl linkers at the 1'-position of the sugar residues were synthesized and incorporated into oligonucleotides, then intercalating groups such as an anthraquinone derivative and a pyrene derivative were attached to the amino groups. Duplexes consisting of
Tetrahedron Letters, 45, 509-509 (2004)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 302309-250MG | 04061837656385 |
| 302309-1G | 04061837656378 |
| 302309-5G | 04061826665831 |

