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2-(3-(hydroxymethyl)phenyl)isoindoline-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92789-55-4

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92789-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92789-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,8 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92789-55:
(7*9)+(6*2)+(5*7)+(4*8)+(3*9)+(2*5)+(1*5)=184
184 % 10 = 4
So 92789-55-4 is a valid CAS Registry Number.

92789-55-4Relevant academic research and scientific papers

Preparation of acetals from aldehydes and alcohols under basic conditions

Grabowski, Jakub,Granda, Jaros?aw M.,Jurczak, Janusz

, p. 3114 - 3120 (2018)

A new, simple protocol for the synthesis of acetals under basic conditions from non-enolizable aldehydes and alcohols has been reported. Such reactivity is facilitated by a sodium alkoxide along with a corresponding trifluoroacetate ester, utilizing formation of sodium trifluoroacetate as a driving force for acetal formation. The usefulness of this protocol is demonstrated by its orthogonality with various acid-sensitive protecting groups and by good compatibility with functional groups, delivering synthetically useful acetals complementarily to the synthesis under acidic conditions from aldehydes and alcohols.

Design, synthesis, and pharmacological evaluation of novel hybrid compounds to treat sickle cell disease symptoms

Dos Santos, Jean Leandro,Lanaro, Carolina,Lima, Ldia Moreira,Gambero, Sheley,Franco-Penteado, Carla Fernanda,Alexandre-Moreira, Magna Suzana,Wade, Marlene,Yerigenahally, Shobha,Kutlar, Abdullah,Meiler, Steffen E.,Costa, Fernando Ferreira,Chung, Manchin

experimental part, p. 5811 - 5819 (2011/10/09)

A novel series of thalidomide derivatives (4a-f) designed by molecular hybridization were synthesized and evaluated in vitro and in vivo for their potential use in the oral treatment of sickle cell disease symptoms. Compounds 4a-f demonstrated analgesic, anti-inflammatory, and NO-donor properties. Compounds 4c and 4d were considered promising candidate drugs and were further evaluated in transgenic sickle cell mice to determine their capacity to reduce the levels of the proinflammatory cytokine tumor necrosis factor α (TNFα). Unlike hydroxyurea, the compounds reduced the concentrations of TNFα to levels similar to those induced with the control dexamethasone (300 μMol/kg). These compounds are novel lead drug candidates with multiple beneficial actions in the treatment of sickle cell disease symptoms and offer an alternative to hydroxyurea treatment.

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