766305
Bis(2-cyanoethyl)-N,N-diisopropylphosphoramidite
95%
동의어(들):
Bis(2-cyanoethoxy)(diisopropylamino)phosphine, Bis(2-cyanoethoxy)-N,N-diisopropylaminophosphine
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C12H22N3O2P
CAS Number:
Molecular Weight:
271.30
MDL number:
UNSPSC 코드:
12352200
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
95%
양식
liquid
refractive index
n20/D 1.465
density
1.039 g/mL at 25 °C
저장 온도
−20°C
SMILES string
CC(C)N(C(C)C)P(OCCC#N)OCCC#N
InChI
1S/C12H22N3O2P/c1-11(2)15(12(3)4)18(16-9-5-7-13)17-10-6-8-14/h11-12H,5-6,9-10H2,1-4H3
InChI key
LDHWBEHZLFDXCU-UHFFFAOYSA-N
일반 설명
Useful phosphorylating reagent used in oligonucleotide synthesis for adding a terminal phosphate group to the 3′ or 5′ hydroxyl.
애플리케이션
Bis(2-cyanoethyl)-N,N-diisopropylphosphoramidite may be used as a phosphitylating agent during the multi-step synthesis of (-)-1L-chiro-inositol 2,3,5-trisphosphate starting from L-quebrachitol.
관련 제품
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
165.0 °F
Flash Point (°C)
73.9 °C
이미 열람한 고객
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Though medicines that target mRNA are under active investigation, there has been little or no effort to develop mRNA itself as a medicine. Here, we report the synthesis of a 130-nt mRNA sequence encoding a 33-amino-acid peptide that includes the
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Liu C, et al.
Carbohydrate Research, 234, 107-115 (1992)
Marek R Baranowski et al.
Nucleic acids research, 48(15), 8209-8224 (2020-06-10)
The high sensitivity of 19F nucleus to changes in the chemical environment has promoted the use of fluorine-labeled molecular probes to study structure and interactions of nucleic acids by 19F NMR. So far, most efforts have focused on incorporating the
Solid-phase synthesis of a New Diphosphate 5-Aminoimidazole-4-carboxamide Riboside (AICAR) derivative and studies toward cyclic AICAR diphosphate ribose.
D?Errico S, et al.
Molecules (Basel), 16(9), 8110-8118 (2011)
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