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M1014

Sigma-Aldrich

Methyl 3-amino-3-deoxy-α-D-mannopyranoside hydrochloride

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About This Item

经验公式（希尔记法）:
C7H15NO5 · HCl
CAS号:
14133-35-8
分子量:
229.66
MDL编号:
MFCD00058235
UNSPSC代码:
12352201
PubChem化学物质编号:
24896470

表单

solid

储存温度

2-8°C

SMILES字符串

Cl.COC1OC(CO)C(O)C(N)C1O

InChI

1S/C7H15NO5.ClH/c1-12-7-6(11)4(8)5(10)3(2-9)13-7;/h3-7,9-11H,2,8H2,1H3;1H

InChI key

UMFRURBOSLCTIW-UHFFFAOYSA-N

应用

Methyl 3-amino-3-deoxy-α-D-mannopyranoside hydrochloride has been used in a study to assess the importance of the nitrogen protecting group on stereoselectivity.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

历史批次信息供参考:

分析证书(COA)

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David Crich et al.
The Journal of organic chemistry, 72(14), 5183-5192 (2007-06-15)
The highly stereocontrolled synthesis of the 3-amino-3-deoxy-beta-mannopyranosides is achieved by means of thioglycoside donors protected with a 4,6-O-benzylidene or alkylidene acetal and a benzylidene imine group. Among the various nitrogen protecting groups investigated only the Schiff's base was found to

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