Welcome to LookChem.com Sign In|Join Free
  • or
3-BROMO-5-NITROBENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

355134-13-3

Post Buying Request

355134-13-3 Suppliers

Recommended suppliers

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

355134-13-3 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 72, p. 5867, 2007 DOI: 10.1021/jo070477u

Check Digit Verification of cas no

The CAS Registry Mumber 355134-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,1,3 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 355134-13:
(8*3)+(7*5)+(6*5)+(5*1)+(4*3)+(3*4)+(2*1)+(1*3)=123
123 % 10 = 3
So 355134-13-3 is a valid CAS Registry Number.

355134-13-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H64787)  3-Bromo-5-nitrobenzaldehyde, 97+%   

  • 355134-13-3

  • 250mg

  • 353.0CNY

  • Detail
  • Alfa Aesar

  • (H64787)  3-Bromo-5-nitrobenzaldehyde, 97+%   

  • 355134-13-3

  • 1g

  • 1058.0CNY

  • Detail
  • Alfa Aesar

  • (H64787)  3-Bromo-5-nitrobenzaldehyde, 97+%   

  • 355134-13-3

  • 5g

  • 4234.0CNY

  • Detail
  • Aldrich

  • (702986)  3-Bromo-5-nitrobenzaldehyde  97%

  • 355134-13-3

  • 702986-250MG

  • 724.23CNY

  • Detail
  • Aldrich

  • (702986)  3-Bromo-5-nitrobenzaldehyde  97%

  • 355134-13-3

  • 702986-1G

  • 2,096.64CNY

  • Detail

355134-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-BROMO-5-NITROBENZALDEHYDE

1.2 Other means of identification

Product number -
Other names 5-bromo-3-nitrobenzaldehyde

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:355134-13-3 SDS

355134-13-3Relevant academic research and scientific papers

Mild Darzens Annulations for the Assembly of Trifluoromethylthiolated (SCF3) Aziridine and Cyclopropane Structures

Delost, Michael D.,Njardarson, Jon T.

supporting information, p. 6121 - 6125 (2021/08/16)

We report mild new annulation approaches to trisubstituted trifluoromethylthiolated (SCF3) aziridines and cyclopropanes via Darzens inspired protocols. The products of these anionic annulations, rarely studied previously, possess attractive features rendering them valuable building blocks for synthesis platforms. In this study, trisubstituted acetophenone nucleophiles bearing SCF3 and bromine substituents in their α position were shown to undergo [2 + 1] annulations with vinyl ketones and tosyl-protected imines under mild reaction conditions.

Discovery and Optimization of a Novel Series of Highly Selective JAK1 Kinase Inhibitors

Grimster, Neil P.,Anderson, Erica,Alimzhanov, Marat,Bebernitz, Geraldine,Bell, Kirsten,Chuaqui, Claudio,Deegan, Tracy,Ferguson, Andrew D.,Gero, Thomas,Harsch, Andreas,Huszar, Dennis,Kawatkar, Aarti,Kettle, Jason G.,Lyne, Paul,Read, Jon A.,Rivard Costa, Caroline,Ruston, Linette,Schroeder, Patricia,Shi, Jie,Su, Qibin,Throner, Scott,Toader, Dorin,Vasbinder, Melissa,Woessner, Richard,Wang, Haixia,Wu, Allan,Ye, Minwei,Zheng, Weijia,Zinda, Michael

supporting information, p. 5235 - 5244 (2018/06/11)

Janus kinases (JAKs) have been demonstrated to be critical in cytokine signaling and have thus been implicated in both cancer and inflammatory diseases. The JAK family consists of four highly homologous members: JAK1-3 and TYK2. The development of small-m

Synthesis and biological evaluation of GPR40/FFAR1 agonists containing 3,5-dimethylisoxazole

Yang, Lingyun,Zhang, Jian,Si, Lianghui,Han, Li,Zhang, Bo,Ma, Hui,Xing, Junhao,Zhao, Leilei,Zhou, Jinpei,Zhang, Huibin

, p. 46 - 58 (2016/04/19)

GPR40 is an attractive target due to its glucose-stimulated insulin secretion effect with low risk of causing hypoglycemia, which also can be seen from the clinical studies using TAK-875 (fasiglifam). In the present studies, we discovered a series of anal

Novel metal oxide nanocomposite of Au/CuO-ZnO for recyclable catalytic aerobic oxidation of alcohols in water

Albadi, Jalal,Alihoseinzadeh, Amir,Razeghi, Abdolhosein

, p. 1 - 5 (2014/03/21)

CuO-ZnO supported gold nanoparticle is introduced as a new, efficient, and recyclable catalyst for the aerobic oxidation of alcohols. The CuO-ZnO support was prepared by co-precipitation and Au nanoparticles were loaded on support by a deposition-precipitation method. The catalyst was characterized by XRD, BET surface area, FESEM, EDS and HRTEM techniques. A wide range of alcohols, including benzylic, primary and secondary alcohols are converted into the corresponding carbonyl derivatives. The experimental procedure with Au/CuO-ZnO catalyst is quite straightforward and the catalyst is recyclable up to 6 consecutive runs by simple filtration.

2 -ARYLAMINOQUINAZOLINES FOR TREATING PROLIFERATIVE DISEASES

-

Page/Page column 185, (2010/01/12)

The invention provides novel compounds that are inhibitors of PDKI. Also provided are pharmaceutical compositions including the compounds, and methods of treating proliferative diseases, such as cancers, with the compounds or composition.

Bromination of deactivated aromatics: A simple and efficient method

Rajesh,Somasundaram,Saiganesh,Balasubramanian

, p. 5867 - 5869 (2008/02/09)

(Chemical Equation Presented) Highly deactivated aromatic compounds were smoothly monobrominated by treatment with N-bromosuccinimide (NBS) in concentrated H2SO4 medium affording the corresponding bromo derivatives in good yields. Mild reaction conditions and simple workup provides a practical and commercially viable route for the synthesis of bromo compounds of deactivated aromatics.

Covalent assembly of molecular ladders

Hartley, C. Scott,Elliott, Erin L.,Moore, Jeffrey S.

, p. 4512 - 4513 (2007/10/03)

[n]-Rung molecular ladders (n = 3-6) have been prepared by reacting discrete, complimentary m-phenylene ethynylene oligomers using imine formation/exchange. The nanostructures, which in the largest case measure approximately 1.6 × 6.2 nm, have been charac

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 355134-13-3