2-Chloro-2-deoxy-D-glucose

Base Information

• Chemical Name: 2-Chloro-2-deoxy-D-glucose
• CAS No.: 14685-79-1
• Molecular Formula: C₆H₁₁ClO₅
• Molecular Weight: 198.603
• Hs Code.: 29329990
• DSSTox Substance ID: DTXSID40163527
• Nikkaji Number: J1.531.214I
• Wikidata: Q83032446
• ChEMBL ID: CHEMBL1255838
• Mol file: 14685-79-1.mol

Synonyms:2-chloro-2-deoxy-D-glucose;2-chloro-2-deoxyglucose;2-deoxy-2-chloro-D-glucose;ClDG

Chemical Property of 2-Chloro-2-deoxy-D-glucose

Chemical Property:

• Appearance/Colour: nearly colourless solid
• Vapor Pressure: 2.11E-12mmHg at 25°C
• Melting Point: 135-136 °C
• Refractive Index: 1.552
• Boiling Point: 507 °C at 760 mmHg
• PKA: 12.67±0.20(Predicted)
• Flash Point: 260.4 °C
• PSA: 97.99000
• Density: 1.553 g/cm³
• LogP: -2.13230
• Storage Temp.: −20°C
• Sensitive.: Air Sensitive/Hygroscopic
• Solubility.: Acetone (Slightly), Water (Slightly)
• XLogP3: -2.2
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 198.0295011
• Heavy Atom Count: 12
• Complexity: 142

Purity/Quality:

99%, ^*data from raw suppliers

2-Chloro-2-deoxy-D-glucose ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(C(C(C(C(C=O)Cl)O)O)O)O
• Isomeric SMILES: C([C@H]([C@H]([C@@H]([C@H](C=O)Cl)O)O)O)O
• Uses: 2-CHLORO-2-DEOXY-D-GLUCOSE is a D-Glucose (G595000) derivative used in the synthesis of sugar nucleotides and oligosaccharides. 2-Deoxy-2-chloro-D-glucose is a D-Glucose (G595000) derivative used in the synthesis of sugar nucleotides and oligosaccharides.

Technology Process of 2-Chloro-2-deoxy-D-glucose

There total 1 articles about 2-Chloro-2-deoxy-D-glucose which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

O1,O3,O4,O6-tetraacetyl-2-chloro-D-2-deoxy-glucitol → 2-chloro-2-deoxy-D-glucose (14685-79-1)

Guidance literature:

With hydrogenchloride;