D-MYO-INOSITOL 1-MONOPHOSPHATE CYCLOHEXYLAMMONIUM SALT

Base Information

• Chemical Name: D-MYO-INOSITOL 1-MONOPHOSPHATE CYCLOHEXYLAMMONIUM SALT
• CAS No.: 106032-59-1
• Molecular Formula: C12H26NO9P
• Molecular Weight: 359.31
• Mol file: 106032-59-1.mol

Synonyms:D-MYO-INOSITOL 1-MONOPHOSPHATE CYCLOHEXYLAMMONIUM SALT;D-myo-inositol 1-monophosphate;D-myo-inositol 1-monophosphate bis(cyclo -hexylamine) salt S;D-MYO-INOSITOL 1-MONOPHOSPHATE*CYCLOHEXY LAMMONIUM;D-MYO-INOSITOL 1-MONOPHOSPHATE BIS(CYCL&;D-myo-inositol 1-monophosphate bis(cyclohexylamine) salt;D-myo-Inositol 1-monophosphate bis(cyclohexylammonium) salt

Chemical Property of D-MYO-INOSITOL 1-MONOPHOSPHATE CYCLOHEXYLAMMONIUM SALT

Chemical Property:

• Flash Point: 14 °C
• PSA: 203.74000
• LogP: -1.73950
• Storage Temp.: −20°C
• Water Solubility.: Soluble in water

Purity/Quality:

97% ^*data from raw suppliers

D-myo-Inositol-1-phosphate (cyclohexyl ammonium salt) ^*data from reagent suppliers

Safty Information:

• Hazard Codes: F,Xi
• Statements: 11-36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of D-MYO-INOSITOL 1-MONOPHOSPHATE CYCLOHEXYLAMMONIUM SALT

There total 41 articles about D-MYO-INOSITOL 1-MONOPHOSPHATE CYCLOHEXYLAMMONIUM 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: 100.0%

C56H59N2O13P (1447464-01-8) + cyclohexylamine (108-91-8,157973-60-9) → D-myo-inositol-3-phosphate biscyclohexylamine salt (14980-89-3,15065-15-3,16006-20-5,32739-43-8,37170-04-0,53797-24-3,70470-66-5,103529-92-6,106032-58-0,106032-59-1,106707-92-0,111956-21-9,114884-35-4,125356-28-7,126722-33-6)

Guidance literature:

C₅₆H₅₉N₂O₁₃P; With N,O-Bis(trimethylsilyl)trifluoroacetamide; In dichloromethane; at 0 ℃; for 0.0333333h; Inert atmosphere;

With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 ℃; for 0.333333h; Inert atmosphere;

cyclohexylamine; Further stages;

DOI:10.1002/anie.201301092

Reference yield: 96.0%

cyclohexylamine (108-91-8,157973-60-9) + 1-O-diphenylphosphate-2,4,6-tri-O-benzyl-D-myo-inositol (376590-85-1) → D-myo-inositol 1-phosphate biscyclohexylammonium salt (106032-59-1)

Guidance literature:

1-O-diphenylphosphate-2,4,6-tri-O-benzyl-D-myo-inositol; With ammonia; lithium; In tetrahydrofuran;

cyclohexylamine; for 1h; Further stages.;

DOI:10.1021/ja016779+

Reference yield: 36.0%

Phosphoric acid mono-((1R,2R,3R,4S,5R,6S)-2,5-bis-benzyloxy-3,4,6-trihydroxy-cyclohexyl) ester; compound with cyclohexylamine → cyklohexylammonium salt of 4(6)-O-phospho-sn-myoinositol (14980-89-3,15065-15-3,16006-20-5,32739-43-8,37170-04-0,53797-24-3,70470-66-5,103529-92-6,106032-58-0,106032-59-1,106707-92-0,111956-21-9,114884-35-4,125356-28-7,126722-33-6)

Guidance literature:

With hydrogen; palladium; In methanol; water;

upstream raw materials:

myo-inositol 1-phosphate

cyclohexylamine

1-O-diphenylphosphate-2,4,6-tri-O-benzyl-D-myo-inositol

6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-D-myo-inositol