3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL

Base Information

• Chemical Name: 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL
• CAS No.: 90366-30-6
• Molecular Formula: C₁₄H₂₀O₁₀
• Molecular Weight: 348.307
• Mol file: 90366-30-6.mol

Synonyms:(+-)-1.4.5.6-Tetra-O-acetyl-myo-inosit;DL-1,4,5,6-tetra-o-acetyl-myo-inositol;1,4,5,6-tetra-O-acetyl-myo-inositol;[(1R,2R,3R,4R,5R,6R)-2,3,4-triacetyloxy-5,6-dihydroxycyclohexyl] acetate;(2,3,4-triacetyloxy-5,6-dihydroxy-cyclohexyl) acetate;(+-)-1r.2t.3c.4t-Tetraacetoxy-cyclohexandiol-(5c.6c);

Chemical Property of 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL

Chemical Property:

• Vapor Pressure: 3.79E-08mmHg at 25°C
• Melting Point: 112-117°C
• Boiling Point: 402.4°Cat760mmHg
• Flash Point: 138.5°C
• PSA: 145.66000
• Density: 1.38g/cm³
• LogP: -1.55140
• Storage Temp.: -20?C Freezer
• Solubility.: Chloroform

Purity/Quality:

97% ^*data from raw suppliers

3,4,5,6-Tetra-O-acetyl-myo-inositol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL is used in the synthesis of seven novel myo-inositol ferulic acid ester derivatives.

Technology Process of 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL

There total 7 articles about 3,4,5,6-TETRA-O-ACETYL-MYO-INOSITOL 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: 95.0%

1(3),2-di-O-(2-tetrahydropyranyl)-3(1)-4(6),5,6(4)-tetra-O-acetyl-sn-myoinositol (4136-18-9) → 1(3),4(6),5,6(4)-tetra-O-acetyl-sn-myo-inositol (13462-79-8,80953-32-8,90366-30-6,108032-48-0,113973-54-9,113973-61-8)

Guidance literature:

With acetic acid; In chloroform; at 80 ℃; for 1h;

Reference yield: 83.0%

3,4,5,6-tetra-O-acetyl-1,2-O-cyclohexylidene-myo-inositol (39110-61-7,53956-50-6) → 1(3),4(6),5,6(4)-tetra-O-acetyl-sn-myo-inositol (13462-79-8,80953-32-8,90366-30-6,108032-48-0,113973-54-9,113973-61-8)

Guidance literature:

With hydrogenchloride; In water; acetic acid; at 100 ℃; for 0.75h;

DOI:10.1016/0008-6215(85)85015-1

Reference yield:

2-O-(2-tetrahydropyranyl)-1(3),4(6),5,6(4)-tetra-O-acetyl-sn-myoinositol (76690-10-3,76739-95-2,90366-31-7) → 1(3),4(6),5,6(4)-tetra-O-acetyl-sn-myo-inositol (13462-79-8,80953-32-8,90366-30-6,108032-48-0,113973-54-9,113973-61-8)

Guidance literature:

With acetic acid; In chloroform; at 80 ℃; for 1h;

upstream raw materials:

D-myo-inositol

1⁽³⁾,2-di-O-(2-tetrahydropyranyl)-3⁽¹⁾-4⁽⁶⁾,5,6⁽⁴⁾-tetra-O-acetyl-sn-myoinositol

2-O-(2-tetrahydropyranyl)-1⁽³⁾,4⁽⁶⁾,5,6⁽⁴⁾-tetra-O-acetyl-sn-myoinositol

1⁽³⁾-O-(2-tetrahydropyranyl)-3⁽¹⁾,4⁽⁶⁾,5,6⁽⁴⁾-tetra-O-acetyl-sn-myoinositol

Downstream raw materials:

3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-1,4,5,6-tetra-O-acetyl-sn-myo-inositol

1-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol

3,4,6-tri-O-acetyl-1,2-O-(3,4,5,6-tetra-O-acetyl-sn-myoinositol-1-orthoacetyl)-β-D-mannopyranose

3,4,6-tri-O-acetyl-1,2-O-(1,4,5,6-tetra-O-acetyl-sn-myoinositol-3-orthoacetyl)-β-D-mannopyranose

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