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"Furan, 2,2'-(1,2-ethanediyl)bis[5-nitro-" is a complex organic compound with the chemical formula C10H10N2O6. It is a derivative of furan, a heterocyclic compound with a five-membered ring containing four carbon atoms and one oxygen atom. In this specific compound, two furan rings are connected through a 1,2-ethanediyl bridge, and each furan ring has a 5-nitro group attached to it. The nitro groups are electron-withdrawing, which can significantly influence the compound's reactivity and stability. Furan, 2,2'-(1,2-ethanediyl)bis[5-nitro- is likely to be used in advanced chemical research or as an intermediate in the synthesis of more complex molecules, given its structural complexity and the presence of multiple functional groups.

4610-65-5

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4610-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4610-65-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,1 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4610-65:
(6*4)+(5*6)+(4*1)+(3*0)+(2*6)+(1*5)=75
75 % 10 = 5
So 4610-65-5 is a valid CAS Registry Number.

4610-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(5-nitro-2-furyl)ethane

1.2 Other means of identification

Product number -
Other names 5,5'-dinitro-2,2'-ethane-1,2-diyl-bis-furan

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:4610-65-5 SDS

4610-65-5Downstream Products

4610-65-5Relevant academic research and scientific papers

REACTION OF NUCLEOPHILES WITH ELECTRON ACCEPTORS BY SN2 OR SINGLE ELECTRON TRANSFER (S.E.T.) MECHANISMS: THIOLATES AND 2-HALOMETHYL-5-NITROFURANS.

Beadle, Charles D.,Bowman, W. Russell,Prousek, Josef

, p. 4979 - 4982 (2007/10/02)

Thiolates react with 2-halomethyl-5-nitrofurans to yield 5-nitrofurfuryl sulphides by a SN2(C) mechanism, and disulphides and 2-methyl-5-nitrofuran by a SN2(X) mechanism.

ELECTRON TRANSFER PROCESSES. REACTION OF 5-NITROFURYL DERIVATIVES GOING BY ANIONRADICAL MECHANISM

Prousek, Josef

, p. 3347 - 3353 (2007/10/02)

5-nitrofurfuryl nitrate and bromide (1a,b) react with electron donors to give 1,2-bis(5-nitro-2-furyl)ethane (II), 1,2-bis(5-nitro-2-furyl)ethylene (III), 5-nitro-2-methylfurane (IV), products of SRN1 reactions Va, Vb and other derivatives.Formation of the derivatives II to V is discussed on the basis of anionradical mechanism. 5-Nitrobenzyl bromide reacts by a SRN1 reaction with 5-nitrofurfuryl phenyl sulphone (Va) in basic medium to give 1-(5-nitro-2-furyl)-1-phenylsulphonyl-2-(4-nitrophenyl)ethane (VIII) and 1-(5-nitro-2-furyl)-2-(4-nitrophenyl)ethylene (IX).

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