beta-D-Glucopyranose, 1-(dihydrogen phosphate), disodium salt

Base Information

• Chemical Name: beta-D-Glucopyranose, 1-(dihydrogen phosphate), disodium salt
• CAS No.: 83833-15-2
• Molecular Formula: C₆H₁₁O₉P*2Na
• Molecular Weight: 304.101
• European Community (EC) Number: 280-989-5
• UNII: H5UE7E3KQS
• DSSTox Substance ID: DTXSID601003916
• Nikkaji Number: J326.872A
• Mol file: 83833-15-2.mol

Synonyms:83833-15-2;beta-D-Glucopyranose, 1-(dihydrogen phosphate), disodium salt;H5UE7E3KQS;beta-D-Glucopyranose 1-Phosphate Disodium Salt;disodium;[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate;EINECS 280-989-5;UNII-H5UE7E3KQS;SCHEMBL8338356;beta-Glucose-1-phosphate disodium;DCOZWBXYGZXXRX-UZUGEDCSSA-L;DTXSID601003916;Disodium 1-O-phosphonatohexopyranose;.BETA.-GLUCOSE-1-PHOSPHATE DISODIUM;beta-D-Glucopyranose1-PhosphateDisodiumSalt;D90747;.BETA.-D-GLUCOSE 1-PHOSPHATE DISODIUM SALT;.BETA.-D-GLUCOPYRANOSE, 1-(DIHYDROGEN PHOSPHATE), DISODIUM SALT;.BETA.-D-GLUCOPYRANOSE, 1-(DIHYDROGEN PHOSPHATE), SODIUM SALT (1:2)

Chemical Property of beta-D-Glucopyranose, 1-(dihydrogen phosphate), disodium salt

Chemical Property:

• PSA: 172.38000
• LogP: -2.22800
• Storage Temp.: <0°C
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 2
• Exact Mass: 303.99360749
• Heavy Atom Count: 18
• Complexity: 266

Purity/Quality:

98%,99%, ^*data from raw suppliers

beta-D-Glucopyranose 1-Phosphate Disodium Salt >98.0%(HPLC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C1C(C(C(C(O1)OP(=O)([O-])[O-])O)O)O)O.[Na+].[Na+]
• Isomeric SMILES: C([C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)OP(=O)([O-])[O-])O)O)O)O.[Na+].[Na+]

Technology Process of beta-D-Glucopyranose, 1-(dihydrogen phosphate), disodium salt

There total 5 articles about beta-D-Glucopyranose, 1-(dihydrogen phosphate), disodium salt 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:

2,3,4,5-tetra-O-acetyl-D-glucopyranose (3947-62-4,6207-76-7,19235-21-3,22554-70-7,22860-22-6,47339-09-3,57884-82-9,62057-79-8,70191-05-8,109525-54-4,140147-37-1,10343-06-3) → D-glucose-1-phosphate disodium salt (16450-65-0,17364-14-6,32972-46-6,56401-20-8,83833-15-2,93839-96-4,99749-54-9,104990-74-1,112820-40-3,147072-63-7,147072-64-8)

Guidance literature:

Multi-step reaction with 4 steps

1: 97 percent / 1,2,4-triazole / CH₂Cl₂ / 2 h / Ambient temperature

2: 98 percent / 30percent H₂O₂ / tetrahydrofuran / 1.5 h / Ambient temperature

3: H₂, 10percent NaHCO₃ / 5percent Pd/C / ethanol / 10 h / 760.2 Torr / Ambient temperature

4: 1N NaOH / 3 h / Ambient temperature

With 1,2,4-Triazole; sodium hydroxide; hydrogen; dihydrogen peroxide; sodium hydrogencarbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane;

Reference yield:

dibenzyl 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl phosphite (149717-36-2) → D-glucose-1-phosphate disodium salt (16450-65-0,17364-14-6,32972-46-6,56401-20-8,83833-15-2,93839-96-4,99749-54-9,104990-74-1,112820-40-3,147072-63-7,147072-64-8)

Guidance literature:

Multi-step reaction with 3 steps

1: 98 percent / 30percent H₂O₂ / tetrahydrofuran / 1.5 h / Ambient temperature

2: H₂, 10percent NaHCO₃ / 5percent Pd/C / ethanol / 10 h / 760.2 Torr / Ambient temperature

3: 1N NaOH / 3 h / Ambient temperature

With sodium hydroxide; hydrogen; dihydrogen peroxide; sodium hydrogencarbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol;

Reference yield:

dibenzyl 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl phosphate (374726-35-9) → D-glucose-1-phosphate disodium salt (16450-65-0,17364-14-6,32972-46-6,56401-20-8,83833-15-2,93839-96-4,99749-54-9,104990-74-1,112820-40-3,147072-63-7,147072-64-8)

Guidance literature:

Multi-step reaction with 2 steps

1: H₂, 10percent NaHCO₃ / 5percent Pd/C / ethanol / 10 h / 760.2 Torr / Ambient temperature

2: 1N NaOH / 3 h / Ambient temperature

With sodium hydroxide; hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In ethanol;

upstream raw materials:

D-glucose pentaacetate

2,3,4,5-tetra-O-acetyl-D-glucopyranose

dibenzyl 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl phosphite

dibenzyl 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl phosphate

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