Welcome to LookChem.com Sign In|Join Free
  • or
2-(2'-Hydroxy-5'-chlorophenyl)benzoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51589-62-9

Post Buying Request

51589-62-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

51589-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51589-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,8 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51589-62:
(7*5)+(6*1)+(5*5)+(4*8)+(3*9)+(2*6)+(1*2)=139
139 % 10 = 9
So 51589-62-9 is a valid CAS Registry Number.

51589-62-9Downstream Products

51589-62-9Relevant academic research and scientific papers

Photo- and thermochromic spiropyrans 43. Spectral kinetic study of new benzoxazolyl-substituted spirobenzopyrans

Rostovtseva, Irina A.,Solov'Eva, Ekaterina V.,Chernyshev, Anatoly V.,Voloshin, Nikolai A.,Trofimova, Nadezhda S.,Metelitsa, Anatoly V.

, p. 223 - 228 (2015)

[Figure not available: see fulltext.] A series of spiroindolinebenzopyrans was prepared, containing a chelating 1,3-benzoxazole group at position 8 of the benzopyran fragment. These new benzoxazolyl-substituted spirobenzopyrans showed photochromic propert

Highly efficient AgNO3-catalyzed approach to 2-(benzo[d]azol-2-yl)phenols from salicylaldehydes with 2-aminothiophenol, 2-aminophenol and benzene-1,2-diamine

He, Xinwei,Wu, Yuhao,Jin, Wenjing,Wang, Xiaoshun,Wu, Cong,Shang, Yongjia

, (2018/02/13)

A new, convenient and efficient AgNO3-catalyzed strategy for the preparation of 2-(benzo[d]azol-2-yl)phenol derivatives in good to excellent yields (63–98%) is described. The reaction proceeds via condensation/intramolecular nucleophilic addition/oxidation process between substituted salicylaldehydes and 2-aminothiophenol, 2-aminophenol or benzene-1,2-diamine under mild reaction conditions. Notably, this reaction utilizes cheap AgNO3 as a readily available and low-cost benign oxidant at low catalyst loadings with excellent functional group tolerance.

Rhodium(III)-Catalyzed ortho-Heteroarylation of Phenols through Internal Oxidative C-H Activation: Rapid Screening of Single-Molecular White-Light-Emitting Materials

Li, Bijin,Lan, Jingbo,Wu, Di,You, Jingsong

, p. 14008 - 14012 (2016/01/25)

Reported herein is the first example of a transition-metal-catalyzed internal oxidative C-H/C-H cross-coupling between two (hetero)arenes through a traceless oxidation directing strategy. Without the requirement of an external metal oxidant, a wide range of phenols, including phenol-containing natural products, can undergo the coupling with azoles to assemble a large library of highly functionalized 2-(2-hydroxyphenyl)azoles. The route provides an opportunity to rapidly screen white-light-emitting materials. As illustrative examples, two bis(triphenylamine)-bearing 2-(2-hydroxyphenyl)oxazoles, which are difficult to access otherwise, exhibit bright white-light emission, high quantum yield, and thermal stability. Also presented is the first example of the white-light emission, in a single excited-state intramolecular proton transfer system, of 2-(2-hydroxyphenyl)azoles, thus highlighting the charm of C-H activation in the discovery of new organic optoelectronic materials.

Palladium catalyzed Csp2-H activation for direct aryl hydroxylation: The unprecedented role of 1,4-dioxane as a source of hydroxyl radicals

Seth, Kapileswar,Nautiyal, Manesh,Purohit, Priyank,Parikh, Naisargee,Chakraborti, Asit K.

supporting information, p. 191 - 194 (2015/01/09)

A novel strategy for direct aryl hydroxylation via Pd-catalysed Csp2-H activation through an unprecedented hydroxyl radical transfer from 1,4-dioxane, used as a solvent, is reported with bio relevant and sterically hindered heterocycles and various acyclic functionalities as versatile directing groups.

Synthesis and in vitro antibacterial and antifungal activities of benzoxazole derivatives

Khan, Khalid Mohammed,Karim, Aneela,Ambreen, Nida,Amyn, Afroz,Saied, Sumayya,Ahmed, Aqeel,Perveen, Shahnaz

, p. 894 - 900 (2013/07/26)

The in vitro antibacterial and antifungal activities of twenty-nine (29) benzoxazole derivatives were tested against fifteen Gram-positive and sixteen Gram-negative strains. Out of the twenty-nine compounds, eighteen compounds 3-5, 7-9, 11-13, 15-25 showed a broad range of activity against tested Gram-positive microorganisms, whereas rest of the compounds 6, 10, 14 and 26-31 were found to be completely inactive against all the tested strains of Gram-positive bacteria. Five compounds 8, 11-13, and 15 showed activities against Gram-negative strains whereas the rest were devoid of any activity. Twenty-one (21) out of twenty-nine (29) compounds possessed antifungal activity. The structures of the synthetic compounds were confirmed by IR, EIMS and 1HNMR spectral data.

2-(2'-Hydroxyphenyl)benzothiazoles, -benzoxazoles, and -benzimidazoles for Plastic Scintillation Applications

Pla-Dalmau, Anna

, p. 5468 - 5473 (2007/10/02)

A new series of fluorescent compounds has been tested as dopants for plastic scintillation applications.Several 2-(2'-hydroxyphenyl)benzothiazole, -benzoxazole, and -benzimidazole derivative have been prepared and studied in a polystyrene matrix.Each deri

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 51589-62-9