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2,6-dibromo-4-butylaniline is a chemical compound that belongs to the family of brominated anilines. It is a derivative of aniline with two bromine atoms attached to the 2 and 6 positions of the benzene ring, and a butyl group attached to the 4 position.

10546-66-4

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10546-66-4 Usage

Uses

Used in Pharmaceutical Industry:
2,6-dibromo-4-butylaniline is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2,6-dibromo-4-butylaniline is used as a building block in the production of agrochemicals, such as pesticides and herbicides. Its presence in these compounds can enhance their effectiveness in controlling pests and weeds in agricultural settings.
Used in Dye Industry:
2,6-dibromo-4-butylaniline is used as a key component in the synthesis of dyes. Its ability to absorb and reflect light makes it suitable for creating a wide range of colors in various dye applications.
Used in Organic Compound Production:
2,6-dibromo-4-butylaniline is used as an intermediate in the production of various organic compounds. Its versatile structure allows it to be a valuable precursor in the synthesis of different organic molecules for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10546-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,4 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10546-66:
(7*1)+(6*0)+(5*5)+(4*4)+(3*6)+(2*6)+(1*6)=84
84 % 10 = 4
So 10546-66-4 is a valid CAS Registry Number.

10546-66-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dibromo-4-butylaniline

1.2 Other means of identification

Product number -
Other names 2,6-Dibromo-4-n-butylaniline

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:10546-66-4 SDS

10546-66-4Upstream product

10546-66-4Relevant academic research and scientific papers

Graphene Oxide Promoted Oxidative Bromination of Anilines and Phenols in Water

Ghorpade, Prashant Vasantrao,Pethsangave, Dattatray Appasha,Some, Surajit,Shankarling, Ganapati Subray

, p. 7388 - 7397 (2018)

The mildly acidic and oxidative nature of graphene oxide, with its large surface area available for catalytic activity, has been explored in aromatic nuclear bromination chemistry for the first time. The versatile catalytic activity of graphene oxide (GO) has been used to selectively and rapidly brominate anilines and phenols in water. The best results were obtained at ambient temperatures using molecular bromine in a protocol promoted by oxidative bromination catalyzed by GO; these transformations proceeded with 100% atom economy with respect to bromine and high selectivities for the tribromoanilines and -phenols. Reduced graphene oxide (r-GO) was observed to form after the second recycle (third use) of GO. This technique is also effective with N-bromosuccinimide (NBS) as the brominating reagent. In the case of NBS, reactions were instantaneous and the GO displayed excellent recyclability without any loss of activity over several cycles.

PARTICLES FOR ELECTROPHORETIC DISPLAYS

-

Page/Page column 97, (2012/03/09)

This invention relates to coloured polymer particles preferably with surface functionality for charge retention, a process for their preparation, the use of these particles for the preparation of an electrophoretic device, colour electrophoretic displays comprising such particle, and new polymerisable dyes.

Copper-catalyzed oxybromination and oxychlorination of primary aromatic amines using LiBr or LiCl and molecular oxygen

Menini, Luciano,Da Cruz Santos, Joyce C.,Gusevskaya, Elena V.

experimental part, p. 2052 - 2058 (2009/08/07)

Nuclear oxybromination of unprotected aromatic primary amines catalyzed by copper(II) acetate [Cu(OAc)2] under mild conditions has been developed, in which bromide ions are used as halogenating agents and dioxygen as a final oxidant. The catalyst shows not only high regioselectivity for para- or ortho-isomers but also a remarkable chemoselectivity for monobromination. Oxychlorination of aniline can also be performed under similar conditions, albeit with lower selectivities, with N-phenylacetamide being the main by-product. This simple catalytic method represents ecologically benign and economically attractive synthetic pathway to expensive low-volume aromatic haloamines.

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