61340-09-8

Basic information

• Product Name: 2,4-O-Benzylidene-D-glucitol
• Synonyms: 2,4-O-Benzylidene-D-glucitol
• CAS NO: 61340-09-8
• Molecular Formula: C₁₃H₁₈O₆
• Molecular Weight: 270.28
• Mol File: 61340-09-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 546.6±45.0 °C(Predicted)
• Appearance: /
• Density: 1.358±0.06 g/cm3(Predicted)
• PKA: 13.05±0.70(Predicted)
• CAS DataBase Reference: 2,4-O-Benzylidene-D-glucitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-O-Benzylidene-D-glucitol(61340-09-8)
• EPA Substance Registry System: 2,4-O-Benzylidene-D-glucitol(61340-09-8)

Safety Data

• Hazardous Substances Data: 61340-09-8(Hazardous Substances Data)

Usage

General Description

2,4-O-Benzylidene-D-glucitol, also known as benzylidene sorbitol, is a chemical compound commonly used in the synthesis of chiral ligands and organocatalysts. It is a derivative of sorbitol, a sugar alcohol, and is characterized by the presence of an O-benzylidene functional group. 2,4-O-Benzylidene-D-glucitol has been widely used in organic chemistry for asymmetric catalysis due to its ability to form complexes with transition metals and its chiral properties. It has also been explored for its potential applications in the pharmaceutical and agrochemical industries. Additionally, 2,4-O-Benzylidene-D-glucitol has shown promise in the development of new materials and as a building block for the synthesis of complex organic molecules. Overall, this chemical compound has a wide range of applications and continues to be a topic of interest for researchers in various fields.

Upstream product

• 50-70-4 D-sorbitol 
• 100-52-7 benzaldehyde 
• 61375-96-0 O¹,O³,O⁵,O⁶-tetraacetyl-O²,O⁴-((S)-benzylidene)-D-glucitol 
• 64-17-5 ethanol 
• 64-19-7 acetic acid 
• 61473-59-4 (1S,3S,5R,6R,8R)-5-<(1R)-1,2-dihydroxyethyl>-3,8-diphenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane 

Downstream Products

• 61375-96-0 O¹,O³,O⁵,O⁶-tetraacetyl-O²,O⁴-((S)-benzylidene)-D-glucitol 
• 7464-39-3 1,6-di-O-benzoyl-2,4-O-benzylidene-D-glucitol 
• 13137-66-1 2,4-O-benzylidene-1,6-di-O-tosyl-D-glucitol 
• 141317-08-0 2,4-O-Benzylidene-L-xylose 
• 93164-50-2 O²,O⁴-((S)-benzylidene)-O⁵,O⁶-isopropylidene-D-glucitol 
• 143573-24-4 (1S,3S,5S,6R)-3-Phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decan-5-carboxaldehyde 
• 143573-32-4 (1S,3S,5R,6R)-5-<(1R)-1-Hydroxy-3-butenyl>-3-phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decane 
• 143573-27-7 2-<(2S,4S,5R,6S)-5-Hydroxy-6-hydroxymethyl-2-phenyl-1,3-dioxan-4-yl>-1,3-diphenylimidazolidine 
• 143573-28-8 2-<(1S,3S,5S,6R)-3-Phenyl-2,4,7,9-tetraoxabicyclo<4.4.0>decan-5-yl>-1,3-diphenylimidazolidine 
• 59837-51-3 O²,O⁴-((S)-benzylidene)-O¹-(toluene-4-sulfonyl)-5,6-anhydro-D-glucitol 
• 7464-42-8 O¹,O⁶-dibenzoyl-O²,O⁴;O³,O⁵-((S,S)-dibenzylidene)-D-glucitol 

Relevant articles and documents

Thermal and Rheological Properties of Physical Gels Formed from Benzylidene- D-sorbitol Derivatives

The thermal and Theological properties of gels formed from 2,4-(mono)-O-benzylidene-D-sorbitol (MBS), 1,3 : 2,4-di-O-benzylidene-D-sorbitol (DBS), and 1,3 : 2,4 : 5,6-tri-O-benzylidene-D-sorbitol (TBS) in ethylene glycol (EG) and from DBS in glycerol (GL)