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Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14467-64-2

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14467-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14467-64-2 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 14467-64:
(7*1)+(6*4)+(5*4)+(4*6)+(3*7)+(2*6)+(1*4)=112
112 % 10 = 2
So 14467-64-2 is a valid CAS Registry Number.

14467-64-2SDS

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 1,6-bis(2-nitrophenyl)-1,6-dioxahexane

1.2 Other means of identification

Product number -
Other names 1,4-bis-(2-nitro-phenoxy)-butane

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:14467-64-2 SDS

14467-64-2Relevant academic research and scientific papers

One High-Nuclearity Cd(II)-Yb(III) Nanoring with Near-IR Luminescent Sensing to Antibiotics

Ma, Yanan,Yang, Xiaoping,Shi, Dongliang,Niu, Mengyu,Schipper, Desmond

, p. 16809 - 16813 (2020)

One 12-metal Cd(II)-Yb(III) nanoring, [Cd8Yb4L8(OAc)8]·4OH (1), with a size of 1.2 × 2.8 × 2.8 nm was obtained from a designed flexible salen-type ligand that has eight coordination sites (O and N atoms). The near-IR emission of Yb(III) at 983 nm was detected upon the excitation of ligand-central absorption at 386 nm. This Cd(II)-Yb(III) nanoring exhibits high sensitivity to nitrofuran antibiotics (NFAs) even in the presence of other antibiotics. The quenching constants and limits of detection of NFAs are 2.5 × 104-4.5 × 104 M-1 and 1.5-2.8 μM, respectively.

High-Nuclearity Cd(II)-Nd(III) Nanowheel with NIR Emission Sensing of Metal Cations and Nitro-Based Explosives

Ma, Yanan,Yang, Xiaoping,Niu, Mengyu,Hao, Wenxin,Shi, Dongliang,Schipper, Desmond

, p. 2821 - 2827 (2021)

One Cd-Nd nanowheel [Cd8Nd4L8(OAc)8]·4OH (1, molecular sizes: 1.2 × 2.8 × 2.8 nm) was obtained by using one designed flexible Schiff base ligand containing eight coordination sites. The Schiff base ligand exhibits a hexadentate η1:η2:η1:η1:η2:η1:μ4 coordination mode. The chromogenic Cd/L components are able to transfer energy to Nd(III), leading to the near-infrared (NIR) lanthanide emission of 1. The energy transfer efficiency (ηsens) is calculated to be 39.4%. 1 shows interesting luminescent sensing activity toward metal cations and nitro-based explosives, in particular to Cu(II), Fe(III), Co(II), and 2,4,6-trinitrophenol (TNP) with high sensitivity. The quenching constants of the complex toward Cu(II), Fe(III), Co(II), and TNP respectively are 8.6 × 104, 6.8 × 104, 6.5 × 104, and 2.1 × 105 M-1. The luminescent sensing of the nanowheel to metal cations is able to be explained by chelation enhancement of the quenching (CHEQ) effect, and its high selectivityto TNP is caused by the photoinduced electron transfer process and inner filter effect , even with the existence of other nitro-based explosives.

Facile one-pot synthesis of aliphatic bridged diaryloxy compounds, cyclic and crown ethers under mild conditions

Sakate, Sachin,Kamble, Sumit,Chikate, Rajiv,Rode, Chandrashekhar

, p. 462 - 470 (2017/03/27)

We report here the facile, room temperature, catalyst free, one pot synthesis of aliphatic bridged diaryloxy compounds, cyclic and crown ethers. Anhydrous potassium carbonate (K2CO3) as a mild base along with dimethyl sulfoxide gener

Synthesis, characterization, tautomerism and theoretical study of some new Schiff base derivatives

Türkolu, Gülen,Berber, Halil,Dal, Hakan,?retir, Cemil

scheme or table, p. 1573 - 1583 (2011/10/03)

New Schiff base derivatives were prepared by the condensation of 5-chloro and 5-bromo salicylaldehyde with bis(o-aminophenol)ethers. Five bis(o-nitrophenol)ether compounds were synthesized using some ditosylate, 1,3-dibromopropane and 1,4-dibromobuthane w

SYNTHESIS OF BAPTA-AM ANALOGUES CAPABLE OF ENHANCING THE VASCULAR PRODUCTION OF PROSTACYCLIN

Heilporn, S.,Broeders, F.,Daloze, D.,Braekman, J. C.,Boeynaems, J. M.

, p. 309 - 320 (2007/10/02)

About 30 analogues of BAPTA-AM, a potential antithrombotic agent, have been synthesized and tested for their effect on the production of prostacyclin.None of them was found to be a better enhancher of the production of prostacyclin by aortic endothelial cells than BAPTA-AM itself.The enhancing effect can be produced by compounds unable to chelate Ca2+, thus confirming that it is not related to their buffering capacity for free Ca2+.

Structural Effect on Chelation Selectivity of Alkaline Earth Metal Ions with Aminopolycarboxylate-Type Chelators

Kimura, Takahide,Maruyama, Tetsushi,Okamura, Mutsuo,Sugiyama, Takashi,Ando, Takashi,Ohno, Atsuyoshi

, p. 1615 - 1621 (2007/10/02)

Two derivatives of 1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (H4bapta), in which the distance between the chelating functions is changed, have been synthesized.The structure-interaction relationships of their complexation behavior with alka

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.

CHROMOGENIC CORONANDS. I. C-ARYLCROWN-FORMAZANS OF THE DO-, TRI-, TETRA-, PENTA-, HEXA-, HEPTA-, AND NONANEDECYNE AND DOCOSYNE SERIES

Ostrovskaya, V. M.,D'yakonova, I. A.,Poponova, R. V.,Kozlova, N. P.,Ryabokobylko, Yu. S.,Filatova, M. P.

, p. 1583 - 1588 (2007/10/02)

The 12- to 22-membered dibenzodi(oligo)oxatetraazacoronands containing a crown-ether fragment and an endocyclic C-arylformazan group (C-arylcrown-formazans) in the ring were obtained by template and nontemplate bisazocoupling of bisdiazotized bis(2-aminoa

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