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Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[3-nitrois a chemical compound that features a benzene ring with 1,1'-[1,4-butanediylbis(oxy)]bis[3-nitrogroups attached. As a nitro compound, it contains nitro functional groups, which are known for their reactivity and potential use in the synthesis of various organic compounds. Due to its chemical structure, it is utilized in a range of industrial applications. However, it is essential to handle Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[3-nitro- with care, as it is toxic and can pose environmental risks if mismanaged.

14467-66-4

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14467-66-4 Usage

Uses

Used in Chemical Synthesis:
Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[3-nitrois used as a key intermediate in the synthesis of various organic compounds. Its nitro groups can be reduced or undergo other chemical reactions to form a wide range of products, making it valuable in the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[3-nitrois utilized as a building block for the development of new drugs. Its unique structure and reactivity allow for the creation of novel compounds with potential therapeutic applications.
Used in Dye and Pigment Industry:
Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[3-nitrois also employed in the dye and pigment industry. Its ability to form colored compounds makes it a useful component in the production of dyes and pigments for various applications, including textiles, plastics, and printing inks.
Used in Environmental Management:
Due to its toxicity and potential environmental impact, Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[3-nitrois used in the development of methods for its safe handling, disposal, and remediation. This includes the design of processes to minimize its release into the environment and the creation of technologies to remediate contaminated sites.

Check Digit Verification of cas no

The CAS Registry Mumber 14467-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,6 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14467-66:
(7*1)+(6*4)+(5*4)+(4*6)+(3*7)+(2*6)+(1*6)=114
114 % 10 = 4
So 14467-66-4 is a valid CAS Registry Number.

14467-66-4SDS

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 1-nitro-3-[4-(3-nitrophenoxy)butoxy]benzene

1.2 Other means of identification

Product number -
Other names 1,4-Bis-m-nitrophenoxybutane

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:14467-66-4 SDS

14467-66-4Relevant academic research and scientific papers

Homo- and hetero-bivalent edrophonium-like ammonium salts as highly potent, dual binding site AChE inhibitors

Leonetti, Francesco,Catto, Marco,Nicolotti, Orazio,Pisani, Leonardo,Cappa, Anna,Stefanachi, Angela,Carotti, Angelo

, p. 7450 - 7456 (2008/12/23)

A number of mono- and bis-quaternary ammonium salts, containing edrophonium-like and coumarin moieties tethered by an appropriate linker, proved to be highly potent and selective dual binding site acetylcholinesterase inhibitors with good selectivity over

Dipole Moments and UV Spectra of some Long-chain Molecules

Baliah, V.,Aparajithan, K.

, p. 255 - 259 (2007/10/02)

About one hundred compounds with long-chain molecular structure have been prepared (most of them are new).The dipole moments of four α,ω-bis(p-methoxyphenylthio)alkanes and five α,ω-bis(p-methoxyphenylsulphonyl)alkanes have been determined to find the effect of chain-length.In the case of sulphones, the observed values are compared with the values calculated for free rotation around all bonds intervening the end dipoles.The uv spectra of some 1,2-(distyrylsulphonyl)ethanes, and a number of α,ω-bis(arylsulphonyl)- and α,ω-bis(aryloxy)alkanes have been recorded to examine the applicability of the principle of chromophore additivity.

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