3945-28-6, 甲基-a-L-吡喃阿拉伯糖苷, Methyl a-L-arabinopyranoside, CAS:3945-28-6

3945-28-6, Methyl a-L-arabinopyranoside,
甲基-a-L-吡喃阿拉伯糖苷,
CAS:3945-28-6
C6H12O5 / 164.156
MFCD09864632

Methyl a-L-arabinopyranoside

甲基-a-L-吡喃阿拉伯糖苷

Methyl a-L-arabinopyranoside is an organic compound that has resonance configurations and can exist in two different stereoisomers. It can be synthesized by reacting 1,2-dichloroethane with glycerol and aqueous sodium hydroxide. The ethers of methyl a-L-arabinopyranoside are catalytic oxidation epoxides. Magnetic resonance analysis of the molecule has been done using nuclear magnetic resonance (NMR). Methylation of the compound will yield methyl ethers, which are obtained by reacting methyl a-L-arabinopyranoside with methanol and sodium methoxide in methanol.

CAS Number	3945-28-6
Product Name	(2R,3R,4S,5S)-2-methoxyoxane-3,4,5-triol
IUPAC Name	(2R,3R,4S,5S)-2-methoxyoxane-3,4,5-triol
Molecular Formula	C6H12O5
Molecular Weight	164.156 g/mol
InChI	InChI=1S/C6H12O5/c1-10-6-5(9)4(8)3(7)2-11-6/h3-9H,2H2,1H3/t3-,4-,5+,6+/m0/s1
InChI Key	ZBDGHWFPLXXWRD-UNTFVMJOSA-N
SMILES	COC1C(C(C(CO1)O)O)O
Synonyms	α-L-Arabinopyranoside Methyl Ether;
Canonical SMILES	COC1C(C(C(CO1)O)O)O
Isomeric SMILES	CO[C@H]1[C@@H]([C@H]([C@H](CO1)O)O)O