671-08-9

Basic information

• Product Name: 2,5-anhydro-D-mannitol-1,6-diphosphate
• Synonyms: 2,5-anhydro-D-mannitol-1,6-diphosphate
• CAS NO: 671-08-9
• Molecular Formula: C6H14O11P2
• Molecular Weight: 324.12
• Mol File: 671-08-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 705.2±70.0 °C(Predicted)
• Appearance: /
• Density: 1.941±0.06 g/cm3(Predicted)
• PKA: 1.55±0.10(Predicted)
• CAS DataBase Reference: 2,5-anhydro-D-mannitol-1,6-diphosphate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-anhydro-D-mannitol-1,6-diphosphate(671-08-9)
• EPA Substance Registry System: 2,5-anhydro-D-mannitol-1,6-diphosphate(671-08-9)

Safety Data

• Hazardous Substances Data: 671-08-9(Hazardous Substances Data)

Usage

Sugar-derived compound

2,5-anhydro-D-mannitol-1,6-diphosphate is a chemical compound derived from sugar.

Metabolism in bacteria and plants

It is involved in the metabolic pathways of certain bacteria and plants.

Derivative of mannitol

It is a derivative of mannitol, a sugar alcohol.

Formation by removal of water molecule

It is formed by the removal of a water molecule from mannitol-1,6-diphosphate.

Intermediate in biosynthesis

It is an important intermediate in the biosynthesis of cell wall components and energy storage molecules in some organisms.

Role and function varies

Its precise role and function may vary depending on the specific organism and metabolic pathway in which it is involved.

Significant role in metabolism and biochemistry

2,5-anhydro-D-mannitol-1,6-diphosphate plays a significant role in the metabolism and biochemistry of certain bacteria and plants.

Upstream product

• 300807-58-3 ((2R,3R,4R,5S)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-methanol 
• 287733-95-3 (2S,3S,4R,5S)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carbaldehyde 
• 162239-10-3 1-deoxy-1-β-ethenyl-2,3,5-tri-O-benzyl-L-xylose 
• 300807-67-4 C₃₀H₃₀O₁₁P₂ 
• 27826-73-9 2,5-anhydro-D-glucitol 

Relevant articles and documents

Synthesis of Selectively Labeled D-Fructose and D-Fructose Phosphate Analogues Locked in the Cyclic Furanose Form

2,5-Anhydroglucitol and 2,5-anhydromannitol and their 6-phosphate and 1,6-diphosphate derivatives are cyclic analogues of the α and β anomers of D-fructofuranose, D-fructofuranose-6-phosphate, and D-fructofuranose-1,6-diphosphate. They were synthesized from protected D-mannose or D-glucose. The synthetic method was developed with emphasis on selective 2H labeling of these compounds, as a model for 3H incorporation, which will be used for further biochemical studies. A key cyclization step, based on a benzyl ether nucleophilic attack on an activated alcohol, constructed the ring system. The stereochemistry at C2 (α/β anomers) and at C5 (D sugar) was controlled by selective epimerizations. Mono- and diphosphate analogues were obtained from the same intermediate by changing the sequence of deprotection and phosphorylation steps.