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重要文件

341096

Sigma-Aldrich

琥珀酰亚胺基 2,2,2-三氯乙基碳酸酯

98%

同義詞:

N-(2,2,2-三氯乙氧基羰基氧基)琥珀酰亚胺

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About This Item

經驗公式(希爾表示法):
C7H6Cl3NO5
CAS號碼:
分子量::
290.49
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

暫時無法取得訂價和供貨情況

化驗

98%

mp

111-113 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

ClC(Cl)(Cl)COC(=O)ON1C(=O)CCC1=O

InChI

1S/C7H6Cl3NO5/c8-7(9,10)3-15-6(14)16-11-4(12)1-2-5(11)13/h1-3H2

InChI 密鑰

WBZXNGAFYBGQFE-UHFFFAOYSA-N

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本產品
HPA075390HPA038832HPA051307
biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

rabbit

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

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Prestige Antibodies® Powered by Atlas Antibodies

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Prestige Antibodies® Powered by Atlas Antibodies

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Prestige Antibodies® Powered by Atlas Antibodies

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Prestige Antibodies® Powered by Atlas Antibodies

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polyclonal

clone

polyclonal

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polyclonal

clone

polyclonal

應用

Succinimidyl 2,2,2-trichloroethyl carbonate was used in the synthesis of:
  • methyl [phenyl 5-(2,2,2-trichloroethoxycarbonylamino)-3,5-dideoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid]-onate[1]
  • phenyl 3,4-di-O-benzyl-6-O-(tert-butyl-dimethyl-silyl)-1-selanyl-2-(2,2,2-trichloroethoxycarbonylamine)-β-D-galactopyranoside[2]

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye 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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分析證明 (COA)

Lot/Batch Number

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Chien-Tai Ren et al.
The Journal of organic chemistry, 72(14), 5427-5430 (2007-06-21)
Synthesis of a tetrasaccharide glycosyl glycerol, the core structure of glycoglycerolipid from Meiothermus taiwanensis ATCC BAA-400, was described. A one-pot glycosylation with three components was employed as a key step.
Chien-Tai Ren et al.
The Journal of organic chemistry, 67(4), 1376-1379 (2002-02-16)
The preparation of a disaccharide 2, Neu5Ac-alpha-(2-->5)Neu5Gc having a alpha-benzyl protecting group at the reducing end, by the coupling of the easily accessible building units 4 and 5 is described. Subsequent deprotection of the coupling adduct led to the isolation

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