60041-69-2

Basic information

• Product Name: Phenol, 2,6-bis(bromomethyl)-, acetate
• CAS NO: 60041-69-2
• Molecular Formula: C10H10Br2O2
• Molecular Weight: 321.996
• Mol File: 60041-69-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phenol, 2,6-bis(bromomethyl)-, acetate(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2,6-bis(bromomethyl)-, acetate(60041-69-2)
• EPA Substance Registry System: Phenol, 2,6-bis(bromomethyl)-, acetate(60041-69-2)

Safety Data

• Hazardous Substances Data: 60041-69-2(Hazardous Substances Data)

Upstream product

• 576-26-1 2.6-dimethylphenol 
• 876-98-2 2,6-dimethylphenyl acetate 

Downstream Products

• 51527-99-2 2,6-bis[N,N-di(2-hydroxyethyl)aminomethyl]phenol 
• 1175002-57-9 {4,10-bis-tert-butoxycarbonylmethyl-7-[2-hydroxy-3-(4,7,10-tris-tertbutoxycarbonylmethyl-1,4,7,10-tetraaza-cyclododec-1-ylmethyl)-benzyl]-1,4,7,10-tetraaza-cyclododec-1-yl}-acetic acid tert-butyl ester 
• 132885-55-3 2,6-Bis-methoxymethyl-4-(4-nitro-phenylazo)-phenol 
• 683199-06-6 2,6-bis(aminomethyl)phenol 
• 481633-15-2 [3-(tert-Butoxycarbonylamino-methyl)-2-hydroxy-benzyl]-carbamic acid tert-butyl ester 
• 183295-28-5 acetic acid 2,6-bis-(tert-butoxycarbonylamino-methyl)-phenyl ester 
• 569643-50-1 2,6-bis((bis((pyridin-2-yl)methyl)amino)methyl)phenol 
• 115289-04-8 N-(2-hydroxyphenyl)methyl-bis(2-pyridylmethyl)amine 
• 852285-97-3 acetic acid 2,6-bis-[(bis-pyridin-2-ylmethyl-amino)-methyl]-phenyl ester 
• 444069-42-5 acetic acid 2-[(bis-pyridin-2-ylmethyl-amino)-methyl]-phenyl ester 

Relevant articles and documents

The synthesis, structure, magnetic and luminescent properties of a new tetranuclear dysprosium (III) cluster

The synthesis and characterization of [Dy4(dhampH 3)4(NO3)2](NO3) 2 (1), a new tetranuclear dysprosium (III) complex, is described. The compound was characterized by its X-ray structure, magnetic properties as well as the luminescent spectra. The compound crystallizes in a P1 space group with a zig-zag linear form of geometry. The ac magnetic susceptibilities of the molecule indicate that it is a magnetic molecule with a slow magnetization relaxation. The molecule also exhibits an emission spectrum that was confirmed to be ligand based. These results indicate that this molecule has both a slow magnetization relaxation (that could be potentially a SMM) and luminescent properties.

Selective anion sensing based on a dual-chromophore approach

A new anion sensor 1 with an azophenol and p-nitrophenyl moieties as chromophores allows for easy colorimetric differentiation of F(-), H2PO4(-) and AcO(-) with similar basicity.

The Synthesis of Ortho-, Meta-, and Paracyclophane- Type Thiacrown Compounds and Their Characteristics as Extractive-Spectrophotometric Reagents for Class b Metals-Silver and Copper

Ortho-, meta-, and paracyclophane-type thiacrown compounds bearing 4-4(nitrophenylazo)phenol as a chromogenic group were synthesized, aand their characteristics as extractive-spectrophotometric reagents for the class b metals, consisting of soft Lewis aci