모든 사진(1)
About This Item
Linear Formula:
[(C2H5)2N]2PCl
CAS Number:
Molecular Weight:
210.68
MDL number:
UNSPSC 코드:
12352001
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
97%
형태
liquid
반응 적합성
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
refractive index
n20/D 1.4895 (lit.)
bp
55-57 °C/0.2 mmHg (lit.)
density
1.002 g/mL at 25 °C (lit.)
작용기
phosphine
SMILES string
CCN(CC)P(Cl)N(CC)CC
InChI
1S/C8H20ClN2P/c1-5-10(6-2)12(9)11(7-3)8-4/h5-8H2,1-4H3
InChI key
JVEHJSIFWIIFHM-UHFFFAOYSA-N
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
보충제 위험성
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
213.8 °F - closed cup
Flash Point (°C)
101 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Synthesis and interactive properties of an oligonucleotide with anthraquinone at the sugar fragment.
K Yamana et al.
Bioconjugate chemistry, 1(5), 319-324 (1990-09-01)
The synthesis of a self-complementary oligonucleotide possessing an anthraquinonylmethyl substituent at the designated sugar fragment, 5'-CCU(2'AQ)AGCTAGG (1), is described. The anthraquinonylmethyl group was introduced to 2'-hydroxyl moiety of uridine, which was then converted to the protected phosphorobisdiethylamidite derivative. This reagent
K Yamana et al.
Nucleic acids symposium series, (21)(21), 31-32 (1989-01-01)
Utilities of deoxyribonucleoside 3'-O-phosphorbisdiethylamidites in the synthesis of oligodeoxyribonucleotides and their analogues are described.
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