362565
双(二乙基氨基)氯膦
97%, liquid
别名:
Chlorobis(diethylamino)phosphine
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关于此项目
线性分子式:
[(C2H5)2N]2PCl
化学文摘社编号:
分子量:
210.68
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.22
MDL number:
产品名称
双(二乙基氨基)氯膦, 97%
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
assay
97%
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
refractive index
n20/D 1.4895 (lit.)
bp
55-57 °C/0.2 mmHg (lit.)
density
1.002 g/mL at 25 °C (lit.)
functional group
phosphine
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
supp_hazards
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
213.8 °F - closed cup
flash_point_c
101 °C - closed cup
ppe
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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