19342-60-0

Basic information

• Product Name: 2-O,4-O:3-O,5-O-Dibenzylidene-D-mannitol
• Synonyms: 2-O,4-O:3-O,5-O-Dibenzylidene-D-mannitol
• CAS NO: 19342-60-0
• Molecular Formula: C₂₀H₂₂O₆
• Molecular Weight: 358.39
• Mol File: 19342-60-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 552.2±45.0 °C(Predicted)
• Appearance: /
• Density: 1.243±0.06 g/cm3(Predicted)
• PKA: 13.71±0.10(Predicted)
• CAS DataBase Reference: 2-O,4-O:3-O,5-O-Dibenzylidene-D-mannitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O,4-O:3-O,5-O-Dibenzylidene-D-mannitol(19342-60-0)
• EPA Substance Registry System: 2-O,4-O:3-O,5-O-Dibenzylidene-D-mannitol(19342-60-0)

Safety Data

• Hazardous Substances Data: 19342-60-0(Hazardous Substances Data)

Upstream product

• 7464-42-8 O¹,O⁶-dibenzoyl-O²,O⁴;O³,O⁵-((Ξ,Ξ)-dibenzylidene)-D-mannitol 
• 13265-77-5 O¹,O⁶-diacetyl-O²,O⁴;O³,O⁵-((S,S)-dibenzylidene)-L-iditol 
• 7464-42-8 O¹,O⁶-dibenzoyl-O²,O⁴;O³,O⁵-((S,S)-dibenzylidene)-D-glucitol 
• 488-44-8 allitol 
• 100-52-7 benzaldehyde 

Downstream Products

• 99436-76-7 2,4:3,5-Di-O-benzyliden-1,6-didesoxy-1,6-diiod-D-mannit 
• 19046-66-3 O²,O⁴;O³,O⁵-((Ξ,Ξ)-dibenzylidene)-1,6-dideoxy-D-mannitol 
• 78465-45-9 O²,O⁴;O³,O⁵-((R,R)-dibenzylidene)-1,6-diiodo-1,6-dideoxy-L-iditol 
• 19046-66-3 O²,O⁴;O³,O⁵-((S,S)-dibenzylidene)-1,6-dideoxy-L-iditol 
• 119073-17-5 O²,O⁴;O³,O⁵-((S,S)-dibenzylidene)-1,6-bis-(2-hydroxy-ethylamino)-1,6-dideoxy-D-glucitol 
• 78481-46-6 O²,O⁴;O³,O⁵-((S,S)-dibenzylidene)-O¹,O⁶-bis-(toluene-4-sulfonyl)-L-iditol 
• 58881-51-9 O²,O³,O⁴,O⁵-tetraacetyl-O¹,O⁶-dibenzoyl-D-iditol 
• 78481-46-6 O²,O⁴;O³,O⁵-((Ξ,Ξ)-dibenzylidene)-O¹,O⁶-bis-(toluene-4-sulfonyl)-D-mannitol 
• 13265-77-5 O¹,O⁶-diacetyl-O²,O⁴;O³,O⁵-((Ξ,Ξ)-dibenzylidene)-D-mannitol 

Relevant articles and documents

Structure Determination of di-O-Benzylidene Derivatives of L-Iditol by 1H and 13C NMR Spectroscopy

The configuration and stable conformation of two dibenzylidene-L-iditol isomers formed upon benzalation of L-iditol, as well as that of a third isomer obtained by partial hydrolysis of the tribenzylidene derivative-the main product of the benzalation reac