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Merck

520330

Sigma-Aldrich

四甲基氟代脲六氟磷酸酯

97%

别名:

TFFH

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About This Item

线性分子式:
[FC[=N(CH3)2]N(CH3)2]PF6
分子量:
264.12
MDL號碼:
分類程式碼代碼:
12352107
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

反應適用性

reaction type: Coupling Reactions

mp

104-109 °C (lit.)

應用

peptide synthesis

SMILES 字串

F[P-](F)(F)(F)(F)F.CN(C)\C(F)=[N+](/C)C

InChI

1S/C5H12FN2.F6P/c1-7(2)5(6)8(3)4;1-7(2,3,4,5)6/h1-4H3;/q+1;-1

InChI 密鑰

ZAVXOOLKAGPJPI-UHFFFAOYSA-N

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應用

Reagent for synthesis of:
Cationic antimicrobial β-2,2-amino acid derivatives
Philanthotoxin analogues for inhibition of the ionotropic glutamate receptor
Small β-peptidomimetics for antimicrobials
Amine prodrugs of selective neuronal nitric oxide synthase inhibitors

Reagent for:
Selective cyclohexyl-derived imidazopyrazine insulin-like growth factor 1 receptor inhibitors
Hydrazone ligation to assemble multifunctional viral nanoparticles

象形圖

CorrosionExclamation mark

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Anita K Kovács et al.
Frontiers in chemistry, 6, 120-120 (2018-05-05)
A general strategy for the synthesis of N-peptide-6-amino-D-luciferin conjugates has been developed. The applicability of the strategy was demonstrated with the preparation of a known substrate, N-Z-Asp-Glu-Val-Asp-6-amino-D-luciferin (N-Z-DEVD-aLuc). N-Z-DEVD-aLuc was obtained via a hybrid liquid/solid phase synthesis method, in which

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