1360145-97-6 Usage
Uses
Used in Organic Synthesis:
2-[(1R,2R)-2-Hydroxycyclopentyl]-isoindole-1,3-dione is used as a synthetic intermediate for the development of various organic compounds. Its unique structure, featuring a cyclopentyl hydroxy group and an isoindole core, makes it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[(1R,2R)-2-Hydroxycyclopentyl]-isoindole-1,3-dione is utilized as a key component in the synthesis of novel drug candidates. Its incorporation into drug molecules can potentially enhance their pharmacological properties, such as potency, selectivity, and bioavailability, leading to the development of more effective therapeutic agents.
Used in Chemical Research:
2-[(1R,2R)-2-Hydroxycyclopentyl]-isoindole-1,3-dione also finds application in chemical research, where it is employed as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. Its unique structural features make it an attractive candidate for exploring innovative approaches in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1360145-97-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,1,4 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1360145-97:
(9*1)+(8*3)+(7*6)+(6*0)+(5*1)+(4*4)+(3*5)+(2*9)+(1*7)=136
136 % 10 = 6
So 1360145-97-6 is a valid CAS Registry Number.
1360145-97-6Relevant academic research and scientific papers
Cyclic trans-β-amino alcohols: Preparation and enzymatic kinetic resolution
Rouf, Abdul,Gupta, Pankaj,Aga, Mushtaq A.,Kumar, Brijesh,Parshad, Rajinder,Taneja, Subhash C.
, p. 2134 - 2143 (2012/05/04)
Enantioenriched cyclic β-amino alcohols, trans-2-aminocyclohexanols (ee, >99%), trans-2-aminocyclopentanols (ee, >99%), trans-1-amino-2- indanols (ee, >99%) and trans-2-amino-1-indanols (ee, ～98%) were prepared in high yields via an Arthrobacter sp. Lipase/PLAP catalyzed kinetic resolution of racemic phthalimido acetates. The addition of toluene as a co-solvent dramatically improved the hydrolysis and enantioselectivity, whereas for indanols, substrate immobilization on Celite improved the efficacy of the kinetic resolution.
