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2,5-bis(furan-2-ylmethylidene)cyclopentanone is a chemical compound characterized by a molecular formula C15H12O2. It features a cyclic structure with two furan-2-ylmethylidene groups attached to a cyclopentanone ring. 2,5-bis(furan-2-ylmethylidene)cyclopentanone is recognized for its unique structure and reactivity, which makes it a valuable intermediate in the synthesis of complex molecules.

1026-78-4

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1026-78-4 Usage

Uses

Used in Organic Chemistry:
2,5-bis(furan-2-ylmethylidene)cyclopentanone is utilized as a versatile building block for the synthesis of various complex molecules. Its unique structure and reactivity contribute to its importance in this field.
Used in Pharmaceutical Production:
2,5-bis(furan-2-ylmethylidene)cyclopentanone is employed as an intermediate in the production of pharmaceuticals, where its properties can be harnessed to create new and effective drug molecules.
Used in Agrochemical Production:
2,5-bis(furan-2-ylmethylidene)cyclopentanone is also used in the synthesis of agrochemicals, indicating its potential in developing new compounds for agricultural applications.
Used in Materials Science:
Due to its interesting photochemical and photophysical properties, 2,5-bis(furan-2-ylmethylidene)cyclopentanone is of interest for potential applications in materials science, where it could be used to develop new materials with specific properties.
Used in Optoelectronics:
2,5-bis(furan-2-ylmethylidene)cyclopentanone's photophysical properties also make it a candidate for use in optoelectronics, where it could be employed in the development of new optoelectronic devices.
Overall, 2,5-bis(furan-2-ylmethylidene)cyclopentanone has a wide range of potential uses and is a subject of interest in both academic and industrial research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 1026-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1026-78:
(6*1)+(5*0)+(4*2)+(3*6)+(2*7)+(1*8)=54
54 % 10 = 4
So 1026-78-4 is a valid CAS Registry Number.

1026-78-4SDS

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 (2E,5E)-2,5-bis(furan-2-ylmethylidene)cyclopentan-1-one

1.2 Other means of identification

Product number -
Other names 2,5-diformylpyridine

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:1026-78-4 SDS

1026-78-4Downstream Products

1026-78-4Relevant academic research and scientific papers

A facile synthesis of α,α'-bis(substituted benzylidene)cycloalkanones catalyzed by bis(p-ethoxyphenyl)telluroxide(BMPTO) under microwave irradiation

Zheng, Ming,Wang, Longcheng,Shao, Jianguo,Zhong, Qi

, p. 351 - 354 (1997)

The bis(4-methoxyphenyl)telluroxide(BMPTO) catalyzed reaction of cyclopentanone or cyclohexanone with aldehydes brought about the cross-aldol condensation to give the corresponding 2,5-bis(substituted benzylidene)cyclopentanones or 2,6-bis(substituted benzylidene)cyclohexanones in high yield under microwave irradiation in mild conditions. The reaction needs only 5-10 min.

Syntheses and Pyrolysis of Some α,α'-Bis(spiro(4-aryl-1-pyrazoline))cycloalkanones

Rao, CH. Bheemasankara,Raju, P. V. Narasimha

, p. 321 - 327 (2007/10/02)

α,α'-Bis(spiro(4-aryl-1-pyrazoline))cycloalkanones (IIa-m) have been synthesized through cycloaddition of diazomethane to α,α'-diarylidenecycloalkanones (Ia-m) which, in turn, are prepared by the aldol condensation of cyclopentanones and cyclohexanones with arylaldehydes and furfuraldehyde.Pyrolysis of bis-spiro compounds yields methyl dienes (VIa-c, l) with expanded ring systems in some cases and in one case formation of cyclopropane (VIII) without ring expansion is observed.

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