1,2-O-Isopropylidene-D-glucofuranose
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1,2-O-Isopropylidene-D-glucofuranose
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CAS No:
18549-40-1
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Formula:
C9H16O6
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Chemical Name:
1,2-O-Isopropylidene-D-glucofuranose
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Synonyms:
MONOACETONGLUCOSE;ISOPROPYLIDENE-D-GLUCOFURANOSE, 1,2-O-;1,2-O-ISOPROPYLIDENE-A-D-GLUCOFURANOSE;1,2-O-ISOPROPYLIDENE-D-GLUCOFURANOSE;1,2-O-ISOPROPYLIDENE-D-GLUCOFURANOSIDE;1,2-O-Isopropylidene;1,2-Mono-O-isopropylidene-a-d-glucofuranose;1,2-O-(1-Methylethylidene)-a-d-glucofuranose
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CAS No:
1,2-O-Isopropylidene-D-glucofuranose Basic Attributes
220.22
220.22
82670
242-420-9
1697
TSCA listed
White
29329990
Characteristics
88.4
-0.3
White powder.
1.2560 (rough estimate)
159-160 °C(lit.)
321.15°C (rough estimate)
209.3±27.3 °C
1.6000 (estimate)
2-8°C
6.62E-09mmHg at 25°C
-13 º (c=1, H2O)
-20°C
Safety Information
3
Xn
24/25-36-26
Xn
Stable under normal temperatures and pressures.
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
20/21/22-36/37/38
1,2-O-Isopropylidene-D-glucofuranose Use and Manufacturing
D-glucopyranose partially protected by pharmaceutical intermediates, an important chiral building block, can be selectively derivatized at the primary hydroxyl group of 6-OH, or oxidatively remove divaleraldehyde derivatives; directly converted to 5,6 -Anhydride compounds (Mitsunobu reaction); preparation of 3,5-O-benzylidene derivatives
1,2-O-Isopropylidene-alpha-D-glucofuranose is used in method for preparaing Tribenoside.
.alpha.-D-Glucofuranose, 1,2-O-(1-methylethylidene)-: ACTIVE
Computed Properties
Molecular Weight:220.22
XLogP3:-0.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:220.09468823
Monoisotopic Mass:220.09468823
Topological Polar Surface Area:88.4
Heavy Atom Count:15
Complexity:243
Undefined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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1,2-O-Isopropylidene-D-glucofuranose
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