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Merck
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重要文件

M8031

Sigma-Aldrich

Methyl 2,3,4,6-tetra-O-acetyl-β-D-thiogalactopyranoside

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About This Item

經驗公式(希爾表示法):
C15H22O9S
CAS號碼:
分子量::
378.39
MDL號碼:
分類程式碼代碼:
12352201
PubChem物質ID:
暫時無法取得訂價和供貨情況

形狀

solid

儲存溫度

−20°C

SMILES 字串

CS[C@@H]1O[C@H](COC(C)=O)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O

InChI

1S/C15H22O9S/c1-7(16)20-6-11-12(21-8(2)17)13(22-9(3)18)14(23-10(4)19)15(24-11)25-5/h11-15H,6H2,1-5H3/t11-,12+,13+,14-,15+/m1/s1

InChI 密鑰

XWFUCHLBRWBKGN-FQKPHLNHSA-N

應用

Methyl 2,3,4,6-tetra-O-acetyl-β-D-thiogalactopyranoside has been used in a study to assess applications of ionic liquids in carbohydrate chemistry. [1] It has also been used to study thioglycosylation in ionic liquids. [2]

儲存類別代碼

13 - Non 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

Eyeshields, Gloves, type N95 (US)


從最近期的版本中選擇一個:

分析證明 (COA)

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Omar A El Seoud et al.
Biomacromolecules, 8(9), 2629-2647 (2007-08-19)
Ionic liquids (ILs) are composed only of ions. Of special interest to this review are those where at least one ion (the cation) is organic and whose melting points are below or not far above room temperature. ILs are designated
Jianguo Zhang et al.
Beilstein journal of organic chemistry, 2, 12-12 (2006-06-29)
A novel, green chemistry, glycosylation strategy was developed based upon the use of ionic liquids. Research studies demonstrated that thiomethyl glycosides could readily be activated with methyl trifluoromethane sulfonate, using 1-butyl-3-methylimidazolium tetrafluoroborate as a solvent. This green chemistry glycosylation strategy

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