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358819

Sigma-Aldrich

二甲基三甲硅基膦酸酯

95%

别名:

Trimethylsilyl dimethyl phosphite

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About This Item

线性分子式:
(CH3)3SiOP(OCH3)2
CAS号:
36198-87-5
分子量:
182.23
Beilstein:
1849308
EC號碼:
252-908-3
MDL號碼:
MFCD00075439
分類程式碼代碼:
12352100
PubChem物質ID:
24862029
NACRES:
NA.22

化驗

95%

形狀

liquid

折射率

n20/D 1.410 (lit.)

bp

36-37 °C/11 mmHg (lit.)

密度

0.954 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

COP(OC)O[Si](C)(C)C

InChI

1S/C5H15O3PSi/c1-6-9(7-2)8-10(3,4)5/h1-5H3

InChI 密鑰

HWMXPTIFAGBDIK-UHFFFAOYSA-N

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相关类别

應用

Dimethyl trimethylsilyl phosphite may be used in the preparation of:
  • protected phosphoamino acid, Fmoc-Abu(PO3Me2)-OH, used in Fmoc/solid-phase peptide synthesis
  • phosphoenolpyruvate (PEP) via trimethylsilylation, bromination and Perkow reaction
  • sialyl phosphonate
  • sulfonamide phosphonates

象形圖

FlameCorrosion
GHS02,GHS05

訊號詞

Danger

危險聲明

H226,H314

危險分類

Flam. Liq. 3 - Skin Corr. 1B

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

89.6 °F - closed cup

閃點（°C）

32 °C - closed cup

個人防護裝備

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

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分析证书(COA)

Lot/Batch Number
BGBC0187
1452552V
1452552
1357771
046809/1

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Silyl phosphites. Part 20. A facile synthesis of phosphoenolpyruvate and its analogue utilizing in situ generated trimethylsilyl bromide.
Sekine M, et al.
Journal of the Chemical Society. Perkin Transactions 1, 2509-2513 (1982)
Amberlyst-15-Catalyzed Facile Synthesis of a-Amino Phosphonates.
Sudhakar D, et al.
Synthetic Communications, 41(7), 976-980 (2011)
Synthesis of novel CMP-NeuNAc analogues having a glycosyl phosphonate structure.
Imamura M and Hashimoto H.
Tetrahedron Letters, 37(9), 1451-1454 (1996)
J W Perich
International journal of peptide and protein research, 44(3), 288-294 (1994-09-01)
The synthesis of the two 4-phosphono-2-aminobutanoyl-containing peptides, Leu-Arg-Arg-Val-Abu(P)-Leu-Gly-OH.CF3CO2H and Ile-Val-Pro-Asn-Abu(P)-Val-Glu-Glu-OH.CF3CO2H was accomplished by the use of Fmoc-Abu(PO3Me2)-OH in Fmoc/solid-phase peptide synthesis. The protected phosphoamino acid, Fmoc-Abu(PO3Me2)-OH, was prepared from Boc-Asp-OtBu in seven steps, the formation of the C-P linkage being

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