19147-10-5

Basic information

• Product Name: 1,2,3,4,5,6,7-hepta-O-acetylheptitol
• Synonyms: D-glycero-D-galacto-Heptitol, heptaacetate (8CI,9CI)
• CAS NO: 19147-10-5
• Molecular Formula: C₂₁H₃₀O₁₄
• Molecular Weight: 506.4545
• Mol File: 19147-10-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 119 °C
• Boiling Point: 524.1°C at 760 mmHg
• Flash Point: 221.6°C
• Density: 1.261g/cm³
• Vapor Pressure: 4.43E-11mmHg at 25°C
• Refractive Index: 1.467
• CAS DataBase Reference: 1,2,3,4,5,6,7-hepta-O-acetylheptitol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4,5,6,7-hepta-O-acetylheptitol(19147-10-5)
• EPA Substance Registry System: 1,2,3,4,5,6,7-hepta-O-acetylheptitol(19147-10-5)

Safety Data

• Hazardous Substances Data: 19147-10-5(Hazardous Substances Data)

Upstream product

• 488-38-0 L-glycero-D-gulo-heptitol 
• 108-24-7 acetic anhydride 
• 488-38-0 D-glycero-D-gluco-heptitol 
• 488-38-0 D-glycero-L-ido-heptitol 
• 527-06-0 perseitol 
• 488-38-0 L-glycero-D-galacto-heptitol 
• 488-38-0 (2R,3R,4R,5S,6S)-Heptane-1,2,3,4,5,6,7-heptaol 
• 488-38-0 D-glycero-L-gulo-heptitol 
• 488-38-0 volemitol 

Relevant articles and documents

Indonesian medicinal plants. XXIV. Stereochemical structure of perseitol x K+ complex isolated from the leaves of Scurrula fusca (Loranthaceae).

A complex of perseitol (D-glycero-D-galacto-heptitol) and K+ ions in a molar ratio of 20:1 was isolated from the leaves of Scurrula fusca (Loranthaceae), which has been traditionally used for the treatment of cancer in Sulawesi Island, Indonesia. The ster

Synthesis of four diastereomeric octofuranoses from D-glucofuranurono-6,3-lactone via Grignard reactions

Reduction of 5-O-tert-butyldimethylsilyl-1,2-O-isopropylidene-α-D-gluco- (2) and -β-L-idofuranurono-6,3-lactone (3) with diisobutylaluminum hydride (DIBAL-H) to the respective hemiacetal at C-6, followed by reaction with vinylmagnesium bromide in either ether or tetrahydrofuran, gives the corresponding diastereomeric pairs of 7,8-dideoxyoct-7-eno-1,4-furanoses.The configurations of the products at C-6 were determined after oxidative cleavage of the terminal double bond and reduction of the aldehyde by conversion of the resulting heptoses into the known corresponding per-O-acetylated heptitols.