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Usage

Uses

Used in Flavor and Fragrance Industry:
4-Methylthiophene-3-carbaldehyde is used as a flavoring agent and fragrance ingredient due to its strong odor, contributing to the creation of distinct scents and tastes in various consumer products.
Used in Organic Synthesis:
In the field of organic chemistry, 4-methylthiophene-3-carbaldehyde serves as a key building block for synthesizing a wide range of organic compounds, highlighting its importance in the development of new chemical entities.
Used in Pharmaceutical Industry:
4-Methylthiophene-3-carbaldehyde is utilized as an intermediate in the production of pharmaceuticals, playing a crucial role in the synthesis of various medicinal compounds.
Used in Materials Science for Electronic Devices:
4-methylthiophene-3-carbaldehyde has potential applications in the development of materials for electronic devices, making it a valuable component in advancing technology within the electronics industry.
Used as a Reagent in Chemical Reactions:
4-Methylthiophene-3-carbaldehyde also functions as a reagent in various chemical reactions, facilitating important processes in research and industrial applications.

Upstream product

• 30318-99-1 3-bromo-4-methylthiophene 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 197723-96-9 (4-methylthien-3-yl)-1-trityl-imidazol-4-yl-methanol 
• 197723-99-2 1-(4-methyl-thiophen-3-yl)-1-(1-trityl-1H-imidazol-4-yl)-propan-1-ol 
• 197723-98-1 1-(4-methyl-thiophen-3-yl)-1-(1-trityl-1H-imidazol-4-yl)-ethanol 
• 197723-97-0 (4-methylthien-3-yl)-1-trityl-imidazol-4-yl-methanone 

Relevant academic research and scientific papers

Peptidylarginine deiminase inhibitor and application thereof

The invention belongs to the technical field of medicine, and particularly relates to a peptidylarginine deiminase PAD4 inhibitor compound shown in a formula (I) or pharmaceutically acceptable salts,stereoisomers and tautomers thereof, as well as pharmaceutical compositions, pharmaceutical preparations and application thereof. X, Y, R1, R2, R3, R4, R5, R7, R8, R9, ring B and m are as defined in the specification. The compound has inhibitory effect on peptidylarginine deiminase PAD4, and can be used for treating various diseases, such as rheumatoid arthritis, vasculitis, systemic lupus erythematosus, ulcerative colitis, multiple sclerosis, cystic fibrosis, cancer, cutaneous lupus erythematosus, asthma and psoriasis.

HALOGEN-SUBSTITUTED HETEROCYCLIC COMPOUND

A novel α-halogen-substituted thiophene compound or a pharmacologically acceptable salt thereof, which has a potent LPA receptor-antagonist activity and is useful as a medicament is provided. A compound represented by the general formula (I) wherein A represents, a phenyl ring, a thiophene ring, or an isothiazole ring; R1 is the same or different, and represents a halogen atom, or a C1-C3 alkyl group; R2 represents a hydrogen atom, or a C1-C6 alkyl group; p represents an integer of 0 to 5; V represents CR3 wherein R3 represents a hydrogen atom, an amino group, a nitro group, or a C1-C3 alkoxy group, or V represents a nitrogen atom; and X represents a halogen atom, or a salt thereof.

4-?(thien-3-yl)methyl!-imidazole analgesics

Described herein are 4-?(thien-3-yl)methyl!-imidazoles of the formula: STR1 wherein R is hydrogen or methyl, and X is C1-4 alkyl, bromine or chlorine; or STR2 wherein Y is hydrogen, C1-4 alkyl, bromine or chlorine, and Z is C1-4

Diazirine derivatives of aromatic heterocyclic compounds

Compounds of the formula STR1 in which Het represents an optionally substituted aromatic heterocycle having a sulphur or oxygen hetero atom and attached via a ring carbon atom, and X is halogen, alkyl, alkaryl, cyano, alkoxy, mono- or di-alkylamino, acylo

Generation and Trapping of (Thiophen-3-yl)halogenocarbenes from 3-Dihalomethylthiophenes or 3-Chloro-3-(thiophen-3-yl)diazirine

Reaction of 3-dihalogenomethylthiophenes with potassium t-butoxide at 0 deg C generates (thiophen-3-yl)halogenocarbenes, or related carbenoids, which are trapped by simple alkenes to give 1-(thiophen-3-yl)-1-halogenocyclopropanes in moderate to good yield