1H-Isoindole-1,3(2H)-dione, 2-(3-oxocyclopentyl)-

Base Information

• Chemical Name: 1H-Isoindole-1,3(2H)-dione, 2-(3-oxocyclopentyl)-
• CAS No.: 1029691-06-2
• Molecular Formula: C13H11NO3
• Molecular Weight: 229.235
• Hs Code.: 2925190090
• Mol file: 1029691-06-2.mol

Synonyms:1H-Isoindole-1,3(2H)-dione, 2-(3-oxocyclopentyl)-;2-(3-oxocyclopentyl)-1H-Isoindole-1,3(2H)-dione

Chemical Property of 1H-Isoindole-1,3(2H)-dione, 2-(3-oxocyclopentyl)-

Chemical Property:

• Boiling Point: 393.5±35.0 °C(Predicted)
• PKA: -2.33±0.20(Predicted)
• PSA: 54.45000
• Density: 1.419±0.06 g/cm3(Predicted)
• LogP: 1.34210
• Storage Temp.: Sealed in dry,Room Temperature

Purity/Quality:

97% ^*data from raw suppliers

2-(3-oxocyclopentyl)-1H-Isoindole-1,3(2H)-dione ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 1H-Isoindole-1,3(2H)-dione, 2-(3-oxocyclopentyl)-

There total 1 articles about 1H-Isoindole-1,3(2H)-dione, 2-(3-oxocyclopentyl)- 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: 71.0%

phthalimide (136918-14-4,85-41-6) + cyclopent-2-enone (930-30-3) → (+/-)-2-(3-oxocyclopentyl)isoindole-1,3-dione (1029691-06-2)

Guidance literature:

phthalimide; cyclopent-2-enone; In methanol; at 20 ℃; for 18h;

With sodium carbonate; In methanol; water;

Reference yield: 66.0%

(+/-)-2-(3-oxocyclopentyl)isoindole-1,3-dione (1029691-06-2) + 4-hydrazinobenzonitrile hydrochloride (2863-98-1) → (+/-)-2-(1,3-dioxo-1,3-dihydroisoindol-2-yl)-1,2,3,4-tetrahydrocyclopenta[b]indole-7-carbonitrile (1029691-07-3)

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; acetic acid; at 90 - 100 ℃; for 36h;

Reference yield:

(+/-)-2-(3-oxocyclopentyl)isoindole-1,3-dione (1029691-06-2) → C13H17NO3 (1445796-28-0)

Guidance literature:

With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 - 20 ℃;

upstream raw materials:

phthalimide

cyclopent-2-enone

Downstream raw materials:

(+/-)-2-(1,3-dioxo-1,3-dihydroisoindol-2-yl)-1,2,3,4-tetrahydrocyclopenta[b]indole-7-carbonitrile

(S)-(7-cyano-1,2,3,4-tetrahydrocyclopenta[b]indol-2-yl)carbamic acid isopropyl ester

(R,S)-7-bromo-1,2,3,4-tetrahydro-cyclopenta[b]indol-2-ylamine

(7-bromo-1,2,3,4-tetrahydrocyclopenta[b]indol-2-yl)carbamic acid isopropyl ester

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