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Key Documents

316555

Sigma-Aldrich

1,6-脱水-β-D-葡萄糖

99%

同義詞:

左旋葡聚糖

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About This Item

經驗公式(希爾表示法):
C6H10O5
CAS號碼:
分子量::
162.14
Beilstein:
80998
EC號碼:
MDL號碼:
分類程式碼代碼:
12352201
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

99%

形狀

powder or crystals

光學活性

[α]18/D −66°, c = 1 in H2O

顏色

beige

mp

182-184 °C (lit.)

溶解度

water: 50 mg/mL, clear, colorless

SMILES 字串

O[C@H]1[C@H](O)[C@H]2CO[C@H](O2)[C@@H]1O

InChI

1S/C6H10O5/c7-3-2-1-10-6(11-2)5(9)4(3)8/h2-9H,1H2/t2-,3-,4+,5-,6-/m1/s1

InChI 密鑰

TWNIBLMWSKIRAT-VFUOTHLCSA-N

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應用

1,6-脱水-β-D-葡萄糖(左旋葡聚糖)可作为前体用于合成:
  • 1,6-脱水-2,4-二脱氧-β-D-甘油六吡喃糖-3-酮糖。
  • 准直线形(Quasi-linear)聚葡萄糖(PGlc),阳离子开环聚合反应。
  • 吡喃葡萄糖的多氮类似物
  • 3-脱氧-3-氟吡喃半乳糖和乙酰化4-脱氧-4-氟吡喃半乳糖。

其他說明

为了全面了解我们针对客户研究提供的各种单糖产品,建议您访问我们的碳水化合物分类页面。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析證明 (COA)

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存取文件庫

Synthesis of Protected 3-Deoxy-3-fluoro-and 4-Deoxy-4-fluoro-d-galactopyranosides from Levoglucosan
Laine D, et al.
The Journal of Organic Chemistry, 82(9), 4986-4992 (2017)
F Mashayekhy Rad et al.
Chemosphere, 211, 617-623 (2018-08-11)
In the present study, a methodology involving hydrophilic interaction liquid chromatography (HILIC) and electrospray (ESI) tandem mass spectrometry (MS/MS) was developed for measurement of anhydrous monosaccharides as markers for wood burning in atmospheric aerosols, PM10. No extensive sample preparation, other
The controlled synthesis of polyglucose in one-dimensional coordination nanochannels
Kobayashi Y, et al.
Chemical Communications (Cambridge, England), 52(29), 5156-5159 (2016)
Dimitra Balla et al.
Environmental science and pollution research international, 25(13), 12191-12205 (2017-09-10)
Two classes of polar organic compounds, dicarboxylic acids (DCAs) and sugars/sugar anhydrides (S/SAs), were measured in airborne particulate matter in the area of Thessaloniki, northern Greece. The target compounds were measured simultaneously in two particle fractions PM10 and PM2.5 during
Practical synthesis of 1, 6-anhydro-2, 4-dideoxy-β -D-glycero-hexopyranos-3-ulose from levoglucosan
Belyk K, et al.
The Journal of Organic Chemistry, 65(8), 2588-2590 (2000)

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