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Furan, 2,3-dihydro-2,2,4,5-tetraphenyl- is a complex organic compound with the chemical formula C28H22O. It is a derivative of furan, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one oxygen atom. In this specific compound, the furan ring is modified by the addition of four phenyl groups (C6H5), which are attached to the carbon atoms at positions 2, 2, 4, and 5. This molecule is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. Due to its complex structure, it is essential to handle Furan, 2,3-dihydro-2,2,4,5-tetraphenyl- with care and follow proper safety guidelines during its synthesis and use.

1056-32-2

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1056-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1056-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1056-32:
(6*1)+(5*0)+(4*5)+(3*6)+(2*3)+(1*2)=52
52 % 10 = 2
So 1056-32-2 is a valid CAS Registry Number.

1056-32-2SDS

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 2,2,4,5-tetraphenyl-3H-furan

1.2 Other means of identification

Product number -
Other names Furan,2,3-dihydro-2,2,4,5-tetraphenyl

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:1056-32-2 SDS

1056-32-2Relevant academic research and scientific papers

Generation of a Ketocarbenoid from α,α-Dibromodeoxybenzoin by Samarium(II) Di-iodide and its Trapping by Alkene Cycloaddition

Fukuzawa, Shin-ichi,Fujinami, Tatsuo,Sakai, Shizuyoshi

, p. 919 - 920 (1987)

α,α-Dibromodeoxybenzoin reacts with samarium(II) di-iodide and alkenes to give dihydrofuran derivatives, regio- and stereo-selectively.

Copper-Catalyzed Regioselective Synthesis of Multisubstituted Furans by Coupling between Ketones and Aromatic Olefins

Dey, Amrita,Ali, Md Ashif,Jana, Sourav,Hajra, Alakananda

, p. 4812 - 4818 (2017/05/12)

A regioselective synthesis of multisubstituted furan derivatives has been developed via Cu(II)-catalyzed intermolecular annulation of aryl ketones with a wide range of aromatic olefins under ambient air in good yields. This protocol is applicable to both cyclic and acyclic aryl ketones.

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