(-)-Conduritol B

Base Information

• Chemical Name: (-)-Conduritol B
• CAS No.: 80338-90-5
• Molecular Formula: C6H10O4
• Molecular Weight: 146.143
• UNII: 24CB531XHG
• Metabolomics Workbench ID: 64990
• Nikkaji Number: J82.137C
• Wikidata: Q27135702
• Mol file: 80338-90-5.mol

Synonyms:5-cyclohexene-1,2,3,4-tetrol;conduritol A;conduritol B;conduritol B, (1alpha,2alpha,3alpha,4beta)-isomer;conduritol B, (1alpha,2beta,3beta,4alpha)-isomer;conduritol B, (1R-(1alpha,2alpha,3beta,4alpha))-isomer;conduritol C

Chemical Property of (-)-Conduritol B

Chemical Property:

• Boiling Point: 281.9±40.0 °C(Predicted)
• PKA: 13.32±0.70(Predicted)
• PSA: 80.92000
• Density: 1.666±0.06 g/cm3(Predicted)
• LogP: -2.00020
• XLogP3: -2.1
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 146.05790880
• Heavy Atom Count: 10
• Complexity: 129

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(C(C(C1O)O)O)O
• Isomeric SMILES: C1=C[C@H]([C@@H]([C@H]([C@@H]1O)O)O)O

Technology Process of (-)-Conduritol B

There total 113 articles about (-)-Conduritol B 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%

C12H18O4 (1360452-45-4) → (1R,2S,3S,4S)-5-cyclohexene-1,2,3,4-tetrol (526-87-4,4782-74-5,4782-75-6,4782-76-7,4942-61-4,4942-62-5,6090-98-8,7586-48-3,25348-64-5,80338-90-5,123238-09-5,129829-51-2,133319-93-4,137567-79-4,138258-55-6,139559-64-1,140923-39-3,129829-50-1)

Guidance literature:

With hydrogenchloride; In methanol; at 20 ℃; for 4h;

DOI:10.1016/j.bmcl.2012.01.007

Reference yield: 100.0%

(3aS,4R,7R,7aS)-3a,4,7,7a-tetrahydro-2,2-dimethyl-1,3-benzodioxole-4,7-diol (371155-64-5) → (1R,2S,3S,4R)-1,2,3,4,tetrahydroxy-5-cyclohexene (80338-90-5)

Guidance literature:

With acetic acid; at 100 ℃;

DOI:10.1021/ol0164233

Reference yield: 100.0%

(2S,3S)-diacetoxy-(1R,4R)-dihydroxycyclohex-5-ene (252316-80-6) → (1R,2S,3S,4R)-1,2,3,4,tetrahydroxy-5-cyclohexene (80338-90-5)

Guidance literature:

With ammonium hydroxide; In methanol;

DOI:10.1016/S0957-4166(99)00344-4

upstream raw materials:

(-)-(1R,2S,3S,4R)-1,2,3,4-tetraacetoxy-5-cyclohexene

1L-(1,3/2,4)-1,2,3,4-Tetrakis(benzyloxy)-5-cyclohexen

(2S,3S)-diacetoxy-(1R,4R)-dihydroxycyclohex-5-ene

(3aS,4R,7R,7aS)-3a,4,7,7a-tetrahydro-2,2-dimethyl-1,3-benzodioxole-4,7-diol

Downstream raw materials:

(+/-)-1,2,3,4-tetra-O-acetylconduritol E

1,2,3,4,5,6-hexa-O-acetyl-muco-inositol

(+/-)-1L-cyclohexane-1,3/2,4-tetrol

(+/-)-1-bromo-1-deoxyconduritol F