Tetrahydrofurfuryl hydrogen phthalate

Base Information

• Chemical Name: Tetrahydrofurfuryl hydrogen phthalate
• CAS No.: 35395-64-3
• Molecular Formula: C13H14 O5
• Molecular Weight: 250.251
• European Community (EC) Number: 252-541-9
• DSSTox Substance ID: DTXSID70956808
• Nikkaji Number: J260.605D
• Mol file: 35395-64-3.mol

Synonyms:35395-64-3;Tetrahydrofurfuryl hydrogen phthalate;EINECS 252-541-9;SCHEMBL11649952;DTXSID70956808;UVTWTSOAOYEVAL-UHFFFAOYSA-N;NS00057679;2-{[(Oxolan-2-yl)methoxy]carbonyl}benzoic acid;2-(((Tetrahydrofuran-2-yl)methoxy)carbonyl)benzoic acid;1,2-Benzenedicarboxylicacid,1-[(tetrahydro-2-furanyl)methyl]ester

Chemical Property of Tetrahydrofurfuryl hydrogen phthalate

Chemical Property:

• Vapor Pressure: 4.05E-08mmHg at 25°C
• Boiling Point: 428.9°Cat760mmHg
• Flash Point: 165.1°C
• PSA: 72.83000
• Density: 1.279g/cm³
• LogP: 1.72060
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 250.08412354
• Heavy Atom Count: 18
• Complexity: 315

Purity/Quality:

99% ^*data from raw suppliers

TETRAHYDROFURFURYL HYDROGEN PHTHALATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1CC(OC1)COC(=O)C2=CC=CC=C2C(=O)O

Technology Process of Tetrahydrofurfuryl hydrogen phthalate

There total 7 articles about Tetrahydrofurfuryl hydrogen phthalate 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:

(+/-)-phthalic acid mono-tetrahydrofurfuryl ester (35395-64-3) → phthalic acid mono-((S)-tetrahydrofurfuryl ester) (35395-64-3)

Guidance literature:

With brucine;

Reference yield:

Tetrahydrofurfuryl alcohol (97-99-4) → phthalic acid mono-((S)-tetrahydrofurfuryl ester) (35395-64-3)

Guidance literature:

Multi-step reaction with 2 steps

1: pyridine

2: brucine

With pyridine; brucine;

Reference yield:

phthalic anhydride (85-44-9) → phthalic acid mono-((S)-tetrahydrofurfuryl ester) (35395-64-3)

Guidance literature:

Multi-step reaction with 2 steps

1: pyridine

2: brucine

With pyridine; brucine;

upstream raw materials:

Tetrahydrofurfuryl alcohol

phthalic anhydride

Downstream raw materials:

(S)-(tetrahydrofuran-2-yl)methanol

(R)-(tetrahydrofuran-2-yl)methanol

benzoic acid-((R)-tetrahydrofurfuryl ester)