- Tris(
cyanoethyl)phosphine is the
organophosphorus compound with the
formula P(CH2CH2CN)3. It is
white solid that is air stable,
which is
unusual for a...
-
Preferred IUPAC name 3,3′-Azanediyldipropanenitrile
Other names Bis(2-
cyanoethyl)amine
Identifiers CAS
Number 111-94-4 3D
model (JSmol)
Interactive image...
-
Although some
bisamidites were
reported as
thermally unstable compounds, 2-
cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite, the
amidite used to prepare...
-
moiety in the
building block 1 (Scheme 4) and in the
product 3 with 2-
cyanoethyl group. This
precluded the
formation of
oligonucleotides branched at the...
-
silicon MOSFETs Organic insulators (e.g.,
undoped trans-polyacetylene;
cyanoethyl pullulan, CEP), for organic-based FETs. For
devices of
equal current driving...
- of
Michael acceptors. Thus with acrylonitrile, it
reacts to give tris(
cyanoethyl)phosphine: PH3 + 3 CH2=CHZ → P(CH2CH2Z)3 (Z is NO2, CN, or C(O)NH2) Acid...
- 40344 52391-89-6
Cinolazepam 7-chloro-3-hydroxy-5-(2-fluorophenyl)-1-(2-
cyanoethyl)-1H-benzo[e] [1,4]diazepin-2(3H)-one 3033621 75696-02-5 Doxefazepam...
- 0186. Klose, J.; Reese, C. B.; Song, Q. (1997). "Preparation of 2-(2-
cyanoethyl)sulfanyl-1H-isoindole-1,3-(2H)-dione and
related sulfur-transfer agents"...
-
cyanoethylation entails alkylation of the
substrate with 3-chloropropionitrile.
Cyanoethyl is a
protecting group. It is
removed by
treatment with base: RNuCH2CH2CN...
- for the Diels-Alder
reaction is a
reversible (equilibrium) reaction. 2-
cyanoethyl –
removed by mild base. The
group is
widely used in
oligonucleotide synthesis...
