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Key Documents

362565

Sigma-Aldrich

双(二乙基氨基)氯膦

97%

同義詞:

Chlorobis(diethylamino)phosphine

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About This Item

線性公式:
[(C2H5)2N]2PCl
CAS號碼:
分子量::
210.68
MDL號碼:
分類程式碼代碼:
12352001
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

liquid

反應適用性

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

折射率

n20/D 1.4895 (lit.)

bp

55-57 °C/0.2 mmHg (lit.)

密度

1.002 g/mL at 25 °C (lit.)

官能基

phosphine

SMILES 字串

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 密鑰

JVEHJSIFWIIFHM-UHFFFAOYSA-N

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1 - Skin Corr. 1B

安全危害

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

213.8 °F - closed cup

閃點(°C)

101 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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分析證明 (COA)

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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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