13964-15-3

Basic information

• Product Name: L-glycero-L-galacto-Heptitol, 2,6-anhydro-
• Synonyms: L-glycero-L-galacto-Heptitol, 2,6-anhydro-
• CAS NO: 13964-15-3
• Molecular Formula: C₇H₁₄O₆
• Molecular Weight: 194.18246
• Mol File: 13964-15-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: L-glycero-L-galacto-Heptitol, 2,6-anhydro-(CAS DataBase Reference)
• NIST Chemistry Reference: L-glycero-L-galacto-Heptitol, 2,6-anhydro-(13964-15-3)
• EPA Substance Registry System: L-glycero-L-galacto-Heptitol, 2,6-anhydro-(13964-15-3)

Safety Data

• Hazardous Substances Data: 13964-15-3(Hazardous Substances Data)

Usage

General Description

L-glycero-L-galacto-Heptitol, 2,6-anhydro- is a chemical compound that is also known as sedoheptulose. It is a seven-carbon sugar alcohol with a cyclic structure. The compound is a rare sugar that is found in some plants and algae. It is known for its potential as a sweetener and has been studied for its potential health benefits, including its effects on blood sugar levels and insulin resistance. Additionally, L-glycero-L-galacto-Heptitol, 2,6-anhydro- has been studied for its potential applications in the food and pharmaceutical industries due to its unique properties.

Upstream product

• 85011-65-0 β-D-galactopyranosylmethyl p-chlorophenyltriazene 
• 85011-63-8 β-D-galactopyranosylmethyl 3,5-dichlorophenyltriazene 
• 85011-62-7 β-D-galactopyranosylmethyl-p-cyanophenyltriazene 
• 85011-64-9 β-D-galactopyranosylmethyl-3,4-dichlorophenyltriazene 
• 59894-00-7 β-D-galactopyranosylmethyl-(p-nitrophenyl)triazene 

Downstream Products

• 228115-94-4 2,6-anhydro-1,3:5,7-di-O-benzylidene-4-O-toluenesulfonyl-L-glycero-L-galacto-heptitol 
• 228115-96-6 2,6-anhydro-4-azido-1,3:5,7-di-O-benzylidene-4-deoxy-L-glycero-L-gluco-heptitol 
• 71072-13-4 Acetic acid (4aS,8aS,9R,9aS,10aR)-2,7-diphenyl-hexahydro-1,3,6,8,10-pentaoxa-anthracen-9-yl ester 
• 71072-12-3 (4aS,8aR,9R,9aR,10aR)-2,7-Diphenyl-hexahydro-1,3,6,8,10-pentaoxa-anthracen-9-ol 

Relevant articles and documents

Effect of Aryl Substituents on the Kinetics of Inactivation of Glycosidases by Glycosylmethylaryltriazenes: Examination of the 'Suicide' Nature of these Inactivations

The inactivation of the Mg2+-free form of the lacZ-β-galactosidase of Escherichia coli at 25.0 deg C by various β-D-galactopyranosylmethylaryltriazenes resembles the spontaneous, rather than the acid-catalysed decomposition of alkylaryltriazenes in that both the maximum first-order rate constant, and the second-order rate constant, are governed by a negative βlg value at pH 7.0 and at pH 8.0.Less extensive data with the β-xylosidase of Penicillium wortmanni and β-D-xylopyranosylmethylaryltriazenes give a similar result.Although the decomposition of the 2-(β-D-galactopyranosyl)ethyl compounds in aqueous solution is 5-10 fold faster than their lower homologues, β-galactosidase inactivation is 3-13 slower. β-D-Galactopyranosylmethyl-p-nitrophenyltriazene does not inactivate the lectin, RCA ricin.