7353-89-1

Usage

Uses

Used in Pharmaceutical Development:
AKOS B019308 is used as a building block for the synthesis of pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Development:
AKOS B019308 is used as a component in the creation of agrochemicals, aiding in the development of products for agricultural applications such as pest control and crop protection.
Used in Scientific Research:
AKOS B019308 is utilized as a research tool in various scientific studies, enabling the exploration of the biological and chemical properties of oxazole derivatives and their potential applications in different fields.
Used in Drug Discovery:
AKOS B019308 is employed as a valuable tool in drug discovery, assisting researchers in identifying and developing new therapeutic agents with improved efficacy and safety profiles.

Upstream product

• 5380-42-7 thiophene-2-carboxylic acid methyl ester 
• 50-00-0 formaldehyd 
• 107-30-2 chloromethyl methyl ether 
• 150587-19-2 methoxymethoxy chloride 

Downstream Products

• 14756-70-8 Methyl-5-aethyl-5,6-dihydro-4H-thieno<2,3-c>-pyrrol-2-carboxylat 
• 1259287-81-4 methyl 5-[(2-nitrophenyl)sulfonyl]-5,6-dihydro-4H-thieno[2,3-c]pyrrole-2-carboxylate 
• 75-09-2 dichloromethane 
• 7712-05-2 4,6-dihydrothieno[3,4-b]thiophene-2-carboxylic acid 
• 14630-08-1 thieno[3,4-b]thiophene-2-carboxylic acid 
• 14630-09-2 thieno[3,4-b]thiophene-2-carboxylic acid methyl ester 
• 7767-60-4 4,6-Dihydro-thieno[3,4-b]thiophene-2-carboxylic acid methyl ester 
• 28694-68-0 5-oxy-5-phenyl-5,6-dihydro-4H-thieno[2,3-c]pyrrole-2-carboxylic acid methyl ester 
• 28694-73-7 5-phenyl-5H-thieno[2,3-c]pyrrole-2-carboxylic acid methyl ester 
• 14756-71-9 5-Aethyl-5H-thieno<2,3-c>-pyrrol-2-carbonsaeure 
• 28694-69-1 5-phenyl-4,7-dihydro-5H-thieno[3,2-d][1,2]oxazine-2-carboxylic acid methyl ester 
• 28694-61-3 5-phenyl-5,6-dihydro-4H-thieno[2,3-c]pyrrole-2-carboxylic acid methyl ester 
• 28694-60-2 5-(toluene-4-sulfonyl)-5,6-dihydro-4H-thieno[2,3-c]pyrrole-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Fused-heterocycle compound and preparation method thereof

The invention discloses a fused-heterocycle compound and a preparation method thereof. A structural general formula is shown as formula 1, X is selected from S or Se; Y is selected from one of S, Se or O; R1 and R2 are selected from hydrogen or iodine, and R1 and R2 are different; R3 is selected from any one of -OH, -OR4 or a polyether group, wherein R4 is an alkyl of a straight chain or a branched chain of C1-C30 or an alkyl of a straight chain or a branched chain of C1-C30 which is substituted by halogen. A series of reactions and hydrolysis are carried out in order to obtain the compound, and at the same time, an intermediate shown in a formula 2 and a preparation method thereof are provided. The preparation method is simple, raw materials have wide sources, products of each reaction have high yields, and obtained yields of target products are higher; the compound shown in the formula 1 can be applied to synthesis of a semi-conducting polymer, and can be used as parent compounds for synthesis of other fused-heterocycle compounds. Structural modification can be carried out in a plurality of modes for the middle shown in the formula 2, so that derivatives with a plurality of structures are obtained.

HETEROCYCLIC COMPOUND AND ORGANIC SOLAR CELL COMPRISING THE SAME

The present specification provides a heterocyclic compound and an organic solar cell comprising the same. In addition, the present specification comprises: a first electrode; a second electrode provided opposite to the first electrode; and one or more organic material layers which are provided between the first electrode and the second electrode and include a photoactive layer.COPYRIGHT KIPO 2016

Semiconducting polymers

Novel semiconducting photovoltaic polymers with conjugated units that provide improved solar conversion efficiency that can be used in electro-optical and electric devices. The polymers exhibit increased solar conversion efficiency in solar devices.

SUBSTITUTED HYDROXAMIC ACIDS AND USES THEREOF

This invention provides compounds of formula (/): wherein R1, R2, G, n, p and q have values as described in the specification, useful as inhibitors of HDAC6. The invention also provides pharmaceutical compositions comprising the comp

SIMPLE PREPARATION OF METHYL 4-CHLOROMETHYL- AND METHYL 5-CHLOROMETHYL-2-THIOPHENECARBOXYLATE

Selective reduction of a mixture of methyl 4-chloromethyl-2-thiophenecarboxylate (I) and the 5-chloromethyl isomer II, prepared by chloromethylation of methyl 2-thiophenecarboxylate (III), gave pure 4-chloromethyl derivative I and 5-methyl-2-thiophenecarboxylate (V) which on treatment with sulfuryl chloride was converted into the 5-chloromethyl isomer II.