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Merck

ALD00598

Sigma-Aldrich

CITU

≥95%

别名:

1,1,3,3-Tetramethyl-2-(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)isouronium
hexafluorophosphate(V)

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About This Item

经验公式(希尔记法):
C13H12Cl4F6N3O3P
分子量:
545.03
分類程式碼代碼:
12352200
NACRES:
NA.22

品質等級

化驗

≥95%

形狀

powder

反應適用性

reaction type: Coupling Reactions

一般說明

CITU is an efficient coupling reagent used in solid and solution phase peptide synthesis, particularly, in acylation and decarboxylative cross-coupling reactions. It can also be used as an activator in the Ni-catalyzed Negishi arylation, alkenylation, alkylation, and alkynylation reactions.

象形圖

Skull and crossbones

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 3 Oral

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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CITU: a peptide and decarboxylative coupling reagent
deGruyter JN, et al.
Organic Letters, 19(22), 6196-6199 (2017)

商品

Novabiochem®可提供大量的偶联剂用于原位活化。原位活化试剂易于使用 - 即使是利用空间位阻氨基酸,并且它们的使用通常没有副反应。

Novabiochem® coupling reagents for in situ activation are fast-reacting and compatible with various amino acids.

相关内容

The Baran Group works with Sigma-Aldrich in providing a portfolio of zinc-based reagents promoting difluoromethylation, trifluoromethylation, trifluoroethylation and isopropylation of aryl and heteroaryl motifs. Baran’s lab has also helped introduce a portable desaturase (Tz0Cl), which promotes the installation of alcohol and amine groups and leaves behind a highly useful tosyl group for further transformations.

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