26116-10-9

Basic information

• Product Name: N-(2-TETRAHYDROFURANMETHYL)PHTHALIMIDE
• Synonyms: 2-((Tetrahydro-2-furanyl)methyl)-1H-isoindole-1,3(2H)dione;N-(2-TETRAHYDROFURANMETHYL)PHTHALIMIDE;N-(Tetrahydrofurfuryl)phthalimide;2((Tetrahydro-2-Furanyl)Methyl)-1H-Isouindole-1,3(2H)Dione
• CAS NO: 26116-10-9
• Molecular Formula: C₁₃H₁₃NO₃
• Molecular Weight: 231.25
• Mol File: 26116-10-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 370.2°C at 760 mmHg
• Flash Point: 177.7°C
• Appearance: /
• Density: 1.314g/cm³
• Vapor Pressure: 1.13E-05mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: N-(2-TETRAHYDROFURANMETHYL)PHTHALIMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-TETRAHYDROFURANMETHYL)PHTHALIMIDE(26116-10-9)
• EPA Substance Registry System: N-(2-TETRAHYDROFURANMETHYL)PHTHALIMIDE(26116-10-9)

Safety Data

• Hazardous Substances Data: 26116-10-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H13NO3/c15-12-10-5-1-2-6-11(10)13(16)14(12)8-9-4-3-7-17-9/h1-2,5-6,9H,3-4,7-8H2

Upstream product

• 4795-29-3 TETRAHYDROFURFURYLAMINE 
• 201230-82-2 carbon monoxide 
• 85-44-9 phthalic anhydride 
• 3003-84-7 Tetrahydrofurfuryl chloride 
• 1074-82-4 potassium phtalimide 

Downstream Products

• 58960-19-3 2-{[5-oxotetrahydrofuran-2-yl]methyl}-1H-isoindole-1,3(2H)-dione 
• 92632-81-0 5-phthalimidyl levulinic acid 
• 5451-09-2 5-aminolevulinic acid hydrochloride 

Relevant articles and documents

Preparation method of 5 -aminolevulinic acid hydrochloride intermediate (by machine translation)

The invention relates to a preparation method of 5 -aminolevulinic acid hydrochloride intermediate, which belongs to the field of pharmaceutical compound synthesis and provides a 5 -aminolevulinic acid hydrochloride intermediate preparation method which comprises the following technical points: (a), (1) or (2) compound in reaction solvent a, oxidizing agent a, compound of formula (5); or process b) wherein the compound of formula (6) or formula (3 4) is obtained under the action of a reaction solvent b and an oxidizing agent b 6. The compound of formula (6) is then purified to give 5 -aminolevulinic acid hydrochloride by an acidic hydrolysis deprotecting group, or a direct acidic hydrolysis deprotecting group. The environment-friendly oxidation reagent is adopted, the quality requirement of high-quality medicine raw materials can be met at the same time, the production efficiency can be improved, and the requirement of industrial large-scale production can be met. (by machine translation)

Preparation method of 5-aminolevulinic acid and Use of the same

The present invention refers to 5-aminolevulinic acid or 5-aminolevulinic acid novel manufacturing method and 5-aminolevulinic acid or a pharmaceutically acceptable salts, for the treatment of skin diseases relates to the use. Synthesis of 5-aminolevulinic acid salt the present invention according to 5-aminolevulinic acid or features a previously known method being much high yield than synthetic method, heavy metals nor chlorine, boron intermediates halogen such as single plate, do not is not synchronized residual product, organic solvent as a solvent in addition a solvent soluble instead, more wound on a clean roll and a.. And the present invention according to 5-aminolevulinic acid or a pharmaceutically acceptable salt by comprising, as an active ingredient for treatment or treatment skin disease gel system or the like, and number lotion composition is topically applied to the skin disease site more excellent the active mode, and for conserving having electrode and the ground of the diode, skin diseases in particular psoriasis alarm healing therapeutic agent for a disease is constructed based on the character data useful for the development can be used..

A New Synthesis of 5-Aminolevulinic Acid

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