260558-15-4

Usage

Uses

Used in Pharmaceutical Industry:
4-Bromo-2-iodotoluene is used as a key intermediate in the synthesis of various pharmaceutical compounds for its reactivity in organic reactions. It aids in the formation of complex organic molecules, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Bromo-2-iodotoluene is utilized as a precursor in the production of various agrochemicals. Its reactivity in organic reactions enables the synthesis of compounds that can be used in the development of pesticides, herbicides, and other agricultural chemicals to improve crop yield and protect against pests.
Used in Organic Synthesis:
4-Bromo-2-iodotoluene is used as a versatile building block in organic synthesis for its ability to participate in palladium-catalyzed coupling reactions. This allows for the formation of a wide range of complex organic molecules, which can be further utilized in various chemical and industrial applications.
Used in Research and Development:
In research and development, 4-Bromo-2-iodotoluene is employed as a valuable compound for studying organic reactions and exploring new synthetic routes. Its reactivity and properties make it an essential tool for chemists to investigate novel chemical transformations and develop innovative synthetic methods.

InChI:InChI=1/C7H6BrI/c1-5-2-3-6(8)4-7(5)9/h2-4H,1H3

Upstream product

• 106-38-7 para-bromotoluene 
• 67-66-3 chloroform 
• 7553-56-2 iodine 
• 64-19-7 acetic acid 
• 35944-64-0 3-iodo-4-methylaniline 
• 39478-78-9 5-bromo-2-methylaniline 

Downstream Products

• 774608-13-8 (5-bromo-2-methylphenyl)boronic acid 
• 1567220-75-0 (2S)-methyl 2-(7-(4-(allyloxy)-4-methylpiperidin-1-yl)-2-(2‘-chloro-6-methyl-6’-((S)-pent-4-en-2-yloxy)-[1,1‘-biphenyl]-3-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-(tert-butoxy)acetate 
• 1601464-01-0 4-bromo-2-ethynyl-1-vinylbenzene 
• 1601464-10-1 6-bromo-2-(5-bromo-2-vinylphenyl)-1,8b-dihydrobiphenylene 
• 1279129-97-3 5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin-3,7-dicarboxylic acid 
• 1279129-94-0 3,7-bis(phenylethynyl)-5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin 
• 1279129-93-9 3,7-bis(4-methoxyphenyl)-5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin 
• 1279129-91-7 3,7-di(thiophen-2-yl)-5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin 
• 1279129-88-2 3,7-dibromo-5-(2,4,6-tri-tert-butylphenyl)dibenzo[b,f]borepin 
• 1261470-87-4 5-bromo-1-iodo-2-benzaldehyde 

Relevant academic research and scientific papers

Practical method for preparation of 2-[18F]fluoro-4-boronophenylalanine

2 - Containing radioactive isotopes18 F] Fluoro -4 - boronylphenylalanine18 F [FBPA] A process for the preparation of the same. [18 F-FBPA is an efficient target compound by suggesting a precursor and reaction conditions w

METHOD FOR PRODUCING 2-FLUORO-4-BORONO-L-PHENYLALANINE, AND A DERIVATIVE OF 2-FLUORO-4-BORONO-L-PHENYLALANINE

The present invention provides a method for producing 2-fluoro-4-borono-L-phenylalanine, and aderivative of 2-fluoro-4-borono-L-phenylalanine. The invention is to prepare and use a compound represented by the following formula. In the formula, R1/su

INHIBITORS OF IKK-BETA SERINE-THERONINE PROTEIN KINASE

Cyclopentyl(2S,4E)-2-amino-5-{3-[4-carbamoyl-5(carbamoylamino)-2-thienyl]phenyl}pent-4-enoate; Cyclopentyl 5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}-L-norvalinate; Cyclopentyl(2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]-5-m

Functionalized dibenzoborepins as components of small molecule and polymeric π-conjugated electronic materials

We present the synthesis and characterization of dibenzo[b,f]borepins (DBBs) functionalized at the para and meta position with respect to the boron center in order to understand how regiochemical issues influence photophysical and electrochemical properti

BORON-CONTAINING PI-ELECTRON MATERIALS INCORPORATING FORMALLY AROMATIC AND NEUTRAL BOREPIN RINGS

The synthesis, functionalization and characterization of borepin-based extended pi-electron molecules is disclosed. Bulky substituents shielded the vacant boron p-orbitals thus allowing synthetic manipulation and purification under ambient lab conditions.

INHIBITORS OF IKK-β SERINE-THREONINE PROTEIN KINASE

Cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5 (carbamoylamino)-2-thienyl]phenyl}pent-4-enoate; Cyclopentyl 5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]phenyl}-L-norvalinate; Cyclopentyl (2S,4E)-2-amino-5-{3-[4-carbamoyl-5-(carbamoylamino)-2-thienyl]-

ASYMMETRIC MONOANTHRACENE DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENT DEVICE AND ORGANIC ELECTROLUMINESCENT DEVICE UTILIZING THE SAME

Provided are an asymmetric monoanthracene derivative having a specific structure, a material for an organic EL device comprising the above asymmetric monoanthracene derivative and an organic EL device in which an organic thin film layer comprising a single layer or plural layers including a luminescent layer is interposed between a cathode and an anode, wherein at least one of the above organic thin film layers contains the asymmetric monoanthracene derivative described above in the form of a single component or a mixed component. Provided are an organic electroluminescent (EL) device having a high luminous efficiency and a long life, an asymmetric monoanthracene derivative which materializes the same and a material for an organic EL device.

Pyrimidines and uses thereof

The invention relates to pyrimidines and uses thereof, including to inhibit lysophosphatidic acid acyltransferase β (LPAAT-β) activity and/or proliferation of cells such as tumor-cells.

Synthesis, SAR, and antitumor properties of diamino-C,N-diarylpyrimidine positional isomers: Inhibitors of lysophosphatidic acid acyltransferase-β

2,4-Diamino-N4,6-diarylpyrimidines were identified as potent, isoform specific inhibitors of lysophosphatidic acid acyltransferase-β (LPAAT-β). Active inhibitors also blocked proliferation of tumor cell lines in vitro. The effect of 2j in an in