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5447-52-9

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5447-52-9 Usage

Physical form

Yellow solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

Building block for the creation of more complex organic compounds in organic synthesis and medicinal chemistry

Aromatic properties

Highly aromatic due to the presence of benzodioxole groups

Biological interactions

Potential for interactions with biological targets, making it a valuable tool in drug discovery and development research.

Check Digit Verification of cas no

The CAS Registry Mumber 5447-52-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5447-52:
(6*5)+(5*4)+(4*4)+(3*7)+(2*5)+(1*2)=99
99 % 10 = 9
So 5447-52-9 is a valid CAS Registry Number.

5447-52-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-bis(1,3-benzodioxol-5-ylmethylidene)cyclopentan-1-one

1.2 Other means of identification

Product number -
Other names 2,5-dipiperonylidene-cyclopentanone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5447-52-9 SDS

5447-52-9Downstream Products

5447-52-9Relevant articles and documents

Ash of pomegranate peels (APP): A bio-waste heterogeneous catalyst for sustainable synthesis of α,α′-bis(substituted benzylidine)cycloalkanones and 2-arylidene-1-tetralones

Patil, Rupesh C.,Patil, Uttam P.,Jagdale, Ashutosh A.,Shinde, Sachinkumar K.,Patil, Suresh S.

, p. 3527 - 3543 (2020/05/13)

Abstract: α,α′-bis(substituted benzylidene)cycloalkanones were efficiently prepared from variously substituted aldehydes and cycloalkanones in water by using ash of pomegranate peels (APP) as a catalyst. The APP-catalyst was obtained from bio-waste by simple thermal treatment to dry peels of pomegranate fruit and formation of its active phase was confirmed by FT-IR, XRD, XRF, EDX, SEM, DSC-TGA and BET techniques. The analysis revealed that the present catalyst has basic sites which promote the synthesis of desired products. The main attractions of our protocol are utilization of highly abundant bio-waste-derived catalyst and good-to-excellent yield in shortest reaction time. This green protocol was further extended for structurally diverse 2-arylidene-1-tetralones by condensation of equimolar quantity of aromatic aldehydes and 1-tetralone at low temperature. The catalyst could be quantitatively recovered and reused effectively for five times. Graphic abstract: [Figure not available: see fulltext.].

Synthesis and fluorescence properties of α,α'-bis(substituted- benzylidene)cycloalkanones catalyzed by 1-methyl-3(2-(sulfooxy)ethyl)-1h- imidazol-3-ium chloride

Wan, Yu,Chen, Xiu-Mei,Pang, Li-Ling,Ma, Rui,Yue, Cai-Hui,Yuan, Rui,Lin, Wei,Yin, Wei,Bo, Rong-Cheng,Wu, Hui

experimental part, p. 2320 - 2328 (2010/09/10)

-Bis(substituted-benzylidene)cycloalkanones were synthesized via a solvent-free cross-aldol condensation of aromatic aldehydes with cycloalkanones in the presence of a catalytic amount 1-methyl-3(2-(sulfooxy)ethyl)-1H-imidazol- 3-ium chloride at room temperature with excellent yields. The screening for optical properties indicated that the size of cycloalkanone has an influence on the fluorescence emission of products. Products coming from cyclohexanone have stronger fluorescence emission than those from cyclopentanone. Copyrigh

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