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Benzene, 1-(1,2-dibromoethyl)-3-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53534-16-0

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53534-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53534-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,3 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53534-16:
(7*5)+(6*3)+(5*5)+(4*3)+(3*4)+(2*1)+(1*6)=110
110 % 10 = 0
So 53534-16-0 is a valid CAS Registry Number.

53534-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,2-dibromoethyl)-3-nitrobenzene

1.2 Other means of identification

Product number -
Other names 1-(1,2-dibromo-ethyl)-3-nitro-benzene

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:53534-16-0 SDS

53534-16-0Relevant academic research and scientific papers

Dihalogenation of Alkenes Using Combinations of N-Halosuccinimides and Alkali Metal Halides

Barrio, Pablo,García-Pedrero, Olaya,López-Matanza, Pablo,Rodríguez, Félix,Rubio-Presa, Rubén

supporting information, p. 4762 - 4766 (2021/09/10)

A simple, efficient and eco-friendly method for the vicinal dihalogenation of alkenes is described. The reaction is performed with a combination of a N-halosuccinimide and an alkali metal halide using environmentally benign solvents such as acetic acid an

Efficient bromination of olefins, alkynes, and ketones with dimethyl sulfoxide and hydrobromic acid

Song, Song,Li, Xinwei,Sun, Xiang,Yuan, Yizhi,Jiao, Ning

supporting information, p. 3285 - 3289 (2015/06/25)

The oxidative bromination of olefins, alkynes, and ketones has been developed with HBr as the brominating reagent and DMSO as the mild oxidant. The simple conditions, high bromide-atom-economy, as well as easy accessibility and low cost of DMSO and HBr make the present strategy prospective for the synthesis of dibrominated alkanes, dibrominated alkenes and α-bromoketones.

Facile one-pot synthesis of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent

Patil, Rajendra D.,Joshi, Girdhar,Adimurthy, Subbarayappa,Ranu, Brindaban C.

experimental part, p. 2529 - 2532 (2009/09/06)

A new method for the preparation of α-bromoketones from olefins using bromide/bromate couple as a nonhazardous brominating agent has been developed. Several α-bromoketones were successfully prepared from a variety of olefins by this method. This procedure is an alternative to conventional molecular bromine.

Mn(III)-catalyzed synthesis of pyrroles from vinyl azides and 1,3-dicarbonyl compounds

Wang, Yi-Feng,Ton, Kah Kah,Chiba, Shunsuke,Narasaka, Koichi

supporting information; experimental part, p. 5019 - 5022 (2009/05/07)

(Chemical Equation Presented) Polysubstituted N-H pyrroles with a wide variety of substituents were prepared from vinyl azides and 1,3-dicarbonyl compounds by using Mn(III) complexes as catalysts.

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