Glucopyranoside,2-ipr-5-ME phenyl

Base Information

• Chemical Name: Glucopyranoside,2-ipr-5-ME phenyl
• CAS No.: 20772-23-0
• Molecular Formula: C16H24O6
• Molecular Weight: 312.363
• DSSTox Substance ID: DTXSID70874851
• Wikidata: Q82856115
• Mol file: 20772-23-0.mol

Synonyms:GLUCOPYRANOSIDE,2-IPR-5-ME PHENYL;SCHEMBL26261040;DTXSID70874851;CHEBI:181212;SB49308;2-(hydroxymethyl)-6-(5-methyl-2-propan-2-ylphenoxy)oxane-3,4,5-triol

Chemical Property of Glucopyranoside,2-ipr-5-ME phenyl

Chemical Property:

• Vapor Pressure: 1.57E-11mmHg at 25°C
• Melting Point: 94 - 100°C
• Boiling Point: 517.4°Cat760mmHg
• Flash Point: 266.7°C
• PSA: 99.38000
• Density: 1.286g/cm³
• LogP: 0.29710
• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility.: DMSO (Slightly), Methanol (Slightly)
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 312.15728848
• Heavy Atom Count: 22
• Complexity: 350

Purity/Quality:

99%, ^*data from raw suppliers

Thymol-b-D-glucopyranoside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=C(C=C1)C(C)C)OC2C(C(C(C(O2)CO)O)O)O

Technology Process of Glucopyranoside,2-ipr-5-ME phenyl

There total 8 articles about Glucopyranoside,2-ipr-5-ME phenyl 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: 93.0%

thymyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside (117887-62-4) → 5-methyl-2-(1-methylethyl)phenyl-O-β-D-glucopyranoside (20772-23-0)

Guidance literature:

With sodium methylate; In methanol; at 20 ℃; for 12h; Inert atmosphere;

DOI:10.2174/1570178613666160524160916

Reference yield: 23.0%

thymol (89-83-8) + 1-deoxy-1-fluoro-α-D-glucose (2106-10-7) → 5-methyl-2-(1-methylethyl)phenyl-O-β-D-glucopyranoside (20772-23-0)

Guidance literature:

With calcium hydroxide; In water; at 20 ℃; for 1h;

DOI:10.1038/s41557-018-0041-8

Reference yield:

UDP-glucose (133-89-1) + thymol (89-83-8) → 5-methyl-2-(1-methylethyl)phenyl-O-β-D-glucopyranoside (20772-23-0)

Guidance literature:

With glycosyltransferases YdhE bacillus licheniformi; magnesium chloride; In dimethyl sulfoxide; at 30 ℃; for 3h; pH=8.8; Enzymatic reaction;

DOI:10.1021/acs.orglett.9b03040

upstream raw materials:

thymyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

thymol

2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

β-D-glucose pentaacetate

Downstream raw materials:

thymyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

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