90050-59-2

Usage

Uses

Used in Organic Synthesis:
5-Bromo-2-methylbenzaldehyde is used as a building block in organic synthesis for its ability to contribute to the formation of complex organic molecules. Its unique structure allows for a wide range of chemical reactions, facilitating the creation of diverse compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 5-Bromo-2-methylbenzaldehyde is utilized as a key intermediate in the synthesis of various medicinal compounds. Its presence in the molecular structure can influence the pharmacological properties of the final product, contributing to the development of new drugs.
Used in Dye Manufacturing:
5-Bromo-2-methylbenzaldehyde is employed as a reagent in the production of dyes, where its aromatic structure and functional groups are essential for the color characteristics and stability of the dyes.
Used in Fragrance and Flavor Industry:
Leveraging its distinctive odor, 5-Bromo-2-methylbenzaldehyde is used as a component in the creation of fragrances and flavors, adding depth and complexity to the sensory profiles of various products.
Used in Chemical Research:
In academic and industrial research settings, 5-Bromo-2-methylbenzaldehyde serves as a valuable compound for studying chemical reactions and exploring new synthetic pathways, further expanding its applications in the field of chemistry.

InChI:InChI=1/C8H7BrO/c1-6-2-3-8(9)4-7(6)5-10/h2-5H,1H3

Upstream product

• 75-56-9 methyloxirane 
• 30674-80-7 2-Isocyanatoethyl methacrylate 
• 24800-25-7 2-(2-(2-(2-hydroxypropoxy)propoxy)propoxy)propan-1-ol 
• 258886-04-3 (5-bromo-2-methylphenyl)methanol 
• 79669-49-1 5-bromo-2-methylbenzoic acid 
• 529-20-4 2-methylphenyl aldehyde 
• 7460-82-4 diethylene glycol ditosylate 
• 156001-51-3 3-Bromo-6-methyl-benzonitrile 

Downstream Products

• 1010412-93-7 4'-(benzyloxy)-4-methylbiphenyl-3-carbaldehyde 
• 1018719-64-6 C₁₅H₁₂O₃ 
• 1370366-64-5 (Z,Z)-5-(2-methyl-5-bromobenzylidene)-3-phenyl-2-(phenylimino)thiazolidin-4-one 
• 1378465-25-8 (E)-3-(5-bromo-2-methylbenzylidene)-1-cyclohexylpyrrolidin-2-one 
• 1378465-10-1 C₂₁H₁₅BrO₂ 

Relevant academic research and scientific papers

SILANE COUPLING AGENT SYNTHESIS METHOD USING SELECTIVE SINGLE TERMINAL REACTION

PROBLEM TO BE SOLVED: To provide an effective synthesis method of a silane coupling agent using a selective single terminal reaction to a both terminals equivalent compound without using expensive noble metal catalysts such as platinum and palladium in synthesis of novel silane coupling agent for adding high compatibility to a radical polymerizable monomer, and thereby adding high mechanical strength, flexibility (suppleness) and durability. SOLUTION: In a reaction for introducing a functional group only to a single terminal of a both terminals equivalent compound such as 1,10-decane diol for example, a nonuniform emulsion state is formed without adding an organic solvent for dissolving both substrates when reaction substrates are not dissolved each other and a reaction is processed at an emulsion boundary surface thereof. For generating the nonuniform emulsion state, the reaction is proceed at the emulsion boundary surface by using a microreactor element, a flow focusing device, a glass beads filling column or the like. SELECTED DRAWING: Figure 4 COPYRIGHT: (C)2020,JPOandINPIT

Catalyst system for producing polyethylene copolymers in a high temperature solution polymerization process

Catalyst system for producing ethylene copolymers in a high temperature solution process, the catalyst system comprising (i) a metallocene complex of formula (I) wherein M is Hf X is a sigma ligand, L is a bridge of the formula —SiR82—, wherein each R8 is independently a C1-C20-hydrocarbyl, tri(C1-C20-alkyl)silyl, C6-C20-aryl, C7-C20-arylalkyl or C7-C20-alkylaryl n is 0, 1 or 2 R1 and R1′ are the same or can be different and can be a linear or branched C1-C6-alkyl group, R2 and R2′ are the same or are different and are a CH2—R9 group, with R9 being H or linear or branched C1-C6-alkyl group R5 and R5′ are the same or are different and can be H or a linear or branched C1-C6-alkyl group or a OR group, wherein R is a C1-C6-alkyl group R6 and R6′ are the same or are different and can be H or a C(R10)3 group, with R10 being the same or different and R10 can be H or a linear or branched C1-C6-alkyl group or R5 and R6 and/or R5′ and R6′ taken together form an unsubstituted 4-7 membered ring condensed to the benzene ring of the indenyl moiety, and R7 and R7′ can be the same or are different and can be H or a linear or branched C1-C6-alkyl group (ii) an aluminoxane cocatalyst and/or (iii) a boron containing cocatalyst and (iv) optionally an aluminum alkyl compound.

SILANE COUPLING COMPOUNDS AND MEDICAL AND/OR DENTAL CURABLE COMPOSITIONS COMPRISING THE SAME

The present invention relate to a novel silane coupling agent and a medical and/or dental curable composition comprising the same. It is an object of the present invention to provide a novel silane coupling agent that imparts high affinity to a radical polymerizable monomer, thereby imparting high mechanical strength, flexibility and durability when used for a medical and/or dental curable composition, and an inorganic filler surface-treated with the novel silane coupling agent and a novel medical and/or dental curable composition. A silane coupling agent including repeating units such as a urethane bond and polyethylene glycol (ether bond) at a specific position is used.

C-Aryl glucoside SGLT2 inhibitors containing a biphenyl motif as potential anti-diabetic agents

A series of highly active C-aryl glucoside SGLT2 inhibitors containing a biphenyl motif were designed and synthesized for biological evaluation. Among the compounds tested, compound 16l demonstrated high inhibitory activity against SGLT2 (IC50 = 1.9 nM) with an excellent pharmacokinetic profile. Further study indicated that the in vivo efficacy of compound 16l was comparable to that of dapagliflozin, suggesting that further development would be worthwhile.

1H-INDOLE-2-CARBOXYLIC ACID DERIVATIVES USEFUL AS PPAR MODULATORS

The present invention relates to certain indole derivatives that are modulators of PPAR, to processes for their preparation, to pharmaceutical compositions containing them and to their use in medicine.

SMALL ORGANIC MOLECULE REGULATORS OF CELL PROLIFERATION

The present invention makes available methods and reagents for modulating proliferation or differentiation in a cell or tissue comprising contacting the cell with a compound. In certain embodiments, the methods and reagents may be employed to correct or inhibit an aberrant or unwanted growth state, e.g., by antagonizing a normal patched pathway or agonizing smoothened or hedgehog activity.

SMALL ORGANIC MOLECULE REGULATORS OF CELL PROLIFERATION

The present invention makes available methods and reagents for modulating proliferation or differentiation in a cell or tissue comprising contacting the cell with a compound. In certain embodiments, the methods and reagents may be employed to correct or inhibit an aberrant or unwanted growth state, e.g., by antagonizing a normal patched pathway or agonizing smoothened orhedgehog activity.

SMALL ORGANIC MOLECULE REGULATORS OF CELL PROLIFERATION

The present invention makes available methods and reagents for modulating proliferation or differentiation in a cell or tissue comprising contacting the cell with a compound. In certain embodiments, the methods and reagents may be employed to correct or inhibit an aberrant or unwanted growth state, e.g., by antagonizing a normal patched pathway or agonizing smoothened orhedgehog activity.