30002-85-8

Basic information

• Product Name: 2,5-anhydro-3,4-O-(1-methylethylidene)-1-O-[(4-methylphenyl)sulfonyl]pentitol
• CAS NO: 30002-85-8
• Molecular Formula: C₁₅H₂₀O₆S
• Molecular Weight: 328.3807
• Mol File: 30002-85-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 455.2°C at 760 mmHg
• Flash Point: 229.1°C
• Density: 1.242g/cm³
• Vapor Pressure: 4.85E-08mmHg at 25°C
• Refractive Index: 1.517
• CAS DataBase Reference: 2,5-anhydro-3,4-O-(1-methylethylidene)-1-O-[(4-methylphenyl)sulfonyl]pentitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-anhydro-3,4-O-(1-methylethylidene)-1-O-[(4-methylphenyl)sulfonyl]pentitol(30002-85-8)
• EPA Substance Registry System: 2,5-anhydro-3,4-O-(1-methylethylidene)-1-O-[(4-methylphenyl)sulfonyl]pentitol(30002-85-8)

Safety Data

• Hazardous Substances Data: 30002-85-8(Hazardous Substances Data)

Usage

Molecular structure

A complex structure with a pentitol ring, a sulfonyl group at the 1-position, and an isopropylidene group at the 3,4-position.

Sulfonyl group presence

Indicates potential pharmaceutical or biological applications, as sulfonyl-containing compounds have been studied for their anti-inflammatory and anti-microbial properties.

Isopropylidene group

May play a role in the compound's reactivity and stability.

Potential biological activity

The intricate structure and presence of functional groups make this compound an interesting target for further research and investigation.

Upstream product

• 370105-22-9 ((3aS,4R,6aR)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol 
• 2457-99-0 1,4-anhydro-2,3-O-isopropylidene-D,L-ribitol 
• 98-59-9 p-toluenesulfonyl chloride 
• 488-81-3 Adonitol 
• 491-19-0 1,4-anhydro-D,L-ribitol 

Relevant articles and documents

Synthesis and structure of selected quaternary N-(1,4-anhydro-5-deoxy-2,3- O-isopropylidene-D,L-ribitol-5-yl)ammonium salts

The syntheses have been developed for quaternary N-(1,4-anhydro-5-deoxy-2, 3-O-isopropylidene-d,l-ribitol-5-yl)ammonium salts derived from five aromatic amines, pyridine, 2-methylpyridine, 3-carbamoylpyridine, 4-(N,N-dimethylamino) pyridine, and quinoline, as well as two tertiary aliphatic amines, trimethylamine and triethylamine. Reactions of 1,4-anhydro-2,3-O-isopropylidene- 5-O-tosyl-d,l-ribitol with tri-n-propylamine and tri-n-butylamine were unsuccessful. The products were identified on the basis of their 1H and 13C NMR spectra. The structure of N-(1,4-anhydro-5-deoxy-2,3-O- isopropylidene-d,l-ribitol-5-yl)trimethylammonium tosylate was additionally elucidated by X-ray diffractometry.