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About This Item

经验公式(希尔记法):
C7H14O6
CAS Number:
分子量:
194.18
Beilstein:
81566
EC 号:
MDL编号:
UNSPSC代码:
41106212
PubChem化学物质编号:
NACRES:
NA.85
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质量水平

方案

≥99.0% (sum of enantiomers, HPLC)
≥99.0%

表单

powder

旋光性

[α]20/D 77.0 to 82.0°, c = 10% in H2O

分子量

194.18 g/mol

mp

187-195 °C
193-196 °C (lit.)

溶解性

H2O: 0.1 g/mL, clear, colorless

应用

microbiology

SMILES字符串

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

InChI

1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6+,7+/m1/s1

InChI key

HOVAGTYPODGVJG-VEIUFWFVSA-N

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一般描述

Methyl α-D-mannopyranoside is a compound that belongs to the class of organic compounds known as o-glycosyl compounds. It is used for the differentiation of Listeria species, Listeria monocytogenes, Listeria innocua, and Listeria welshimeri can ferment the sugar, producing acid which can be identified using an appropriate pH indicator. It has been used to synthesize a series of tri- and tetrahydroxylated seven-membered imino sugars in a study that worked towards a stable Noeuromycin (glycosyl cation mimic that strongly inhibits glycosidases) analog with a D-manno configuration. It has also been used in a study to investigate the primary mannose-binding site of Pradimicin A. (antifungal agent)

应用

Methyl α-D-mannopyranoside can be used to identify different species of Listeria based on their ability to ferment the sugar.

其他说明

抑制亲和素和内源性凝集素的结合

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

404.1 °F

闪点(°C)

206.74 °C

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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