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2,6-dibromo-4-iodoaniline is a chemical compound with the molecular formula C6H5Br2IN. It is a derivative of aniline, which is a fundamental building block in the production of many industrial chemicals. 2,6-dibromo-4-iodoaniline is a solid at room temperature, characterized by a high melting point, and is insoluble in water but readily soluble in organic solvents. Its chemical properties and versatility make it a valuable component in various applications across different industries.

10527-69-2

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10527-69-2 Usage

Uses

Used in Pharmaceutical Synthesis:
2,6-dibromo-4-iodoaniline is used as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds, contributing to the development of new drugs and therapeutic agents.
Used in Dye Production:
In the dye industry, 2,6-dibromo-4-iodoaniline is employed as a starting material for the production of various dyes. Its chemical properties enable the creation of dyes with specific color characteristics, making it an essential component in the formulation of colorants for textiles, plastics, and other materials.
Used in Organic Chemistry Research:
2,6-dibromo-4-iodoaniline is used as a reagent in various chemical reactions, particularly in the field of organic chemistry. Its presence in reactions can lead to the formation of new compounds with potential applications in research and industry, making it a valuable tool for chemists and researchers.
Used in Chemical Synthesis:
2,6-dibromo-4-iodoaniline is utilized in the synthesis of a variety of organic compounds, including those used in the production of specialty chemicals, agrochemicals, and other industrial products. Its versatility in chemical reactions makes it a sought-after compound in the chemical synthesis process.

Check Digit Verification of cas no

The CAS Registry Mumber 10527-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,2 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10527-69:
(7*1)+(6*0)+(5*5)+(4*2)+(3*7)+(2*6)+(1*9)=82
82 % 10 = 2
So 10527-69-2 is a valid CAS Registry Number.

10527-69-2Relevant academic research and scientific papers

Combining Synthesis and Self-Assembly in One Pot to Construct Complex 2D Metallo-Supramolecules Using Terpyridine and Pyrylium Salts

Wang, Heng,Li, Yiming,Yu, Hao,Song, Bo,Lu, Shuai,Hao, Xin-Qi,Zhang, Yuan,Wang, Ming,Hla, Saw-Wai,Li, Xiaopeng

, p. 13187 - 13195 (2019)

Multicomponent self-assembly in one pot provides an efficient way for constructing complex architectures using multiple types of building blocks with different levels of interactions orthogonally. The preparation of multiple types of building blocks typic

Preparation method of 3, 5-dibromo iodobenzene

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Paragraph 0014; 0015; 0016, (2016/11/24)

The present invention discloses a preparation method of 3, 5-dibromo iodobenzene. The preparation method comprises the following steps: Step 1, p-Iodoaniline and absolute ethyl alcohol are added into a container, and dibromodimethyl hydantoin is added int

Synthesis and optoelectronic properties of janus -dendrimer-type multivalent donor-acceptor systems

Dengiz, Cagatay,Breiten, Benjamin,Gisselbrecht, Jean-Paul,Boudon, Corinne,Trapp, Nils,Schweizer, W. Bernd,Diederich, Fran?ois

, p. 882 - 896 (2015/01/30)

A convergent, multistep protocol was employed for the synthesis of a Janus-type multivalent donor-acceptor system. The synthetic approach is based on a Sonogashira cross-coupling of two differently ferrocene-(Fc) substituted dendrons and a final sixfold [

Palladium-Catalyzed Regioselective Hydrodebromination of Dibromoindoles: Application to the Enantioselective Synthesis of Indolodioxane U86192A

Chae, Junghyun,Buchwald, Stephen L.

, p. 3336 - 3339 (2007/10/03)

A novel approach to the selective preparation of 4-bromoindoles was developed via Pd(OAc)2/rac-BINAP catalytic reactions. A variety of 4,6-dibromoindoles were transformed to 4-bromoindoles with high regioselectivity. This methodology, along wit

Organometallic dendrimers based on (tetraphenylcyclobutadiene)cyclopentadienylcobalt modules

Waybright, Shane M.,McAlpine, Kanika,Laskoski, Matthew,Smith, Mark D.,Bunz, Uwe H. F.

, p. 8661 - 8666 (2007/10/03)

The synthesis and characterization of novel organometallic polyphenylene dendrimers containing 24 or 44 phenyl rings and one cyclobutadiene(cyclopentadienyl)cobalt unit is reported. The dendrimers are made by the convergent CpCo(CO)2-mediated dimerization of di- or tetraethynyltolanes followed by a divergent core extension utilizing tetraphenylcyclopentadienone. The obtained dendrimers are air and water stable, soluble materials that show interesting differences in their hydrodynamic properties as evidenced by gel permeation chromatography. Scanning pulse voltammetry in solution shows that the dendrimers are oxidized at potentials ranging from 0.8 to 0.83 V. The more sterically encumbered the dendrimer, the higher its oxidation potential, that is, the more difficult oxidation is.

Mild and regioselective oxidative bromination of anilines using potassium bromide and sodium perborate

Roche, Didier,Prasad, Kapa,Repic, Oljan,Blacklock, Thomas J.

, p. 2083 - 2085 (2007/10/03)

The selective monobromination of various deactivated anilines using potassium bromide and sodium perborate as oxidant has been achieved. The use of ammonium molybdate as catalyst accelerates the rate of reaction but is not essential to obtain good yields and high selectivities. (C) 2000 Elsevier Science Ltd.

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