14467-64-2

Basic information

• Product Name: Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[2-nitro-
• Synonyms: 1,4-Bis-(2-nitro-phenoxy)-butan;1,4-bis(o-nitrophenoxy)butane;1,4-bis-(2-nitro-phenoxy)-butane
• CAS NO: 14467-64-2
• Molecular Formula: C16H16N2O6
• Molecular Weight: 332.313
• Mol File: 14467-64-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[2-nitro-(14467-64-2)
• EPA Substance Registry System: Benzene, 1,1'-[1,4-butanediylbis(oxy)]bis[2-nitro-(14467-64-2)

Safety Data

• Hazardous Substances Data: 14467-64-2(Hazardous Substances Data)

Upstream product

• 110-52-1 1,4-dibromo-butane 
• 824-39-5 sodium o-nitrophenate 
• 88-75-5 2-hydroxynitrobenzene 
• 100-02-7 4-nitro-phenol 

Downstream Products

• 1329608-96-9 C₃₀H₂₆Cl₂N₂O₄ 
• 129435-33-2 17-(Toluene-4-sulfonyl)-2,7-dioxa-14,17,20-triaza-tricyclo[19.4.0.0^8,13]pentacosa-1⁽²⁵⁾,8⁽¹³⁾,9,11,21,23-hexaene-15,19-dione 
• 129435-36-5 17-(Toluene-4-sulfonyl)-2,7-dioxa-14,17,20-triaza-tricyclo[19.4.0.0^8,13]pentacosa-1⁽²⁵⁾,8⁽¹³⁾,9,11,21,23-hexaene 
• 161554-91-2 [(2-{4-[2-(Bis-ethoxycarbonylmethyl-amino)-phenoxy]-butoxy}-phenyl)-ethoxycarbonylmethyl-amino]-acetic acid ethyl ester 
• 157687-84-8 1,4-bis(o-aminophenoxy)butane-N,N,N',N'-tetraacetic acid 

Relevant articles and documents

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

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.

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

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

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+.