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Benzoxazole, 2-(4-bromophenyl)-5-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112606-72-1

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112606-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112606-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,0 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112606-72:
(8*1)+(7*1)+(6*2)+(5*6)+(4*0)+(3*6)+(2*7)+(1*2)=91
91 % 10 = 1
So 112606-72-1 is a valid CAS Registry Number.

112606-72-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromophenyl)-5-nitro-1,3-benzoxazole

1.2 Other means of identification

Product number -
Other names -

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:112606-72-1 SDS

112606-72-1Relevant academic research and scientific papers

Optically operated second order optical effects in some substituted 4-(5-nitro-1,3-benzoxazol-2-yl)aniline chromophores

Szlachcic,Fedorchuk,Danel,Jarosz,El Naggar,Albassam,Wojciechowski,Gondek,Uchacz,Stadnicka,Lakshminarayana,Kityk

, p. 333 - 341 (2017)

In this work, we report on second order nonlinear optical (NLO) susceptibilities of some substituted 4-(5-nitro-1,3-benzoxazol-2-yl)aniline chromophores that were embedded into photopolymer matrices. Depending on the photo-induced nitrogen laser (waveleng

Deep eutectic solvent-catalyzed arylation of benzoxazoles with aromatic aldehydes

Tran, Phuong Hoang,Thi Hang, Anh-Hung

, p. 11127 - 11133 (2018/03/26)

A novel and efficient methodology for the arylation of benzoxazoles with aromatic aldehydes catalyzed by deep eutectic solvent has been developed. The reaction smoothly proceeded with a wide range of substrates to give the desired products in high yields within short reaction time. Deep eutectic solvents are easily recovered and reused without significant loss of catalytic activity.

Synthesis of Benzoxazoles Using Electrochemically Generated Hypervalent Iodine

Koleda, Olesja,Broese, Timo,Noetzel, Jan,Roemelt, Michael,Suna, Edgars,Francke, Robert

, p. 11669 - 11681 (2017/11/24)

The indirect ("ex-cell") electrochemical synthesis of benzoxazoles from imines using a redox mediator based on the iodine(I)/iodine(III) redox couple is reported. Tethering the redox-active iodophenyl subunit to a tetra-alkylammonium moiety allowed for anodic oxidation to be performed without supporting electrolyte. The mediator salt can be easily recovered and reused. Our "ex-cell" approach toward the electrosynthesis of benzoxazoles is compatible with a range of redox-sensitive functional groups. An unprecedented concerted reductive elimination mechanism for benzoxazole formation is proposed on the basis of control experiments and DFT calculations.

ANTIVIRAL 2-CARBOXY-THIOPHENE COMPOUNDS

-

Page/Page column 51, (2008/06/13)

Anti-viral agents of compounds of Formula (I) : wherein A, R1, R2 and R3 are as defined in the specification, processes for their preparation and their use in HCV treatment are provided.

Parallel synthesis of benzoxazoles via microwave-assisted dielectric heating

Pottorf, Richard S.,Chadha, Naresh K.,Katkevics, Martins,Ozola, Vita,Suna, Edgars,Ghane, Hadi,Regberg, Tor,Player, Mark R.

, p. 175 - 178 (2007/10/03)

A facile route to benzoxazoles has been developed using microwave-assisted dielectric heating. The ease of synthesis and workup allowed the parallel synthesis of a 48-membered library of benzoxazoles quickly and efficiently.

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