439692-90-7

Usage

Uses

Used in Pharmaceutical Industry:
4-CHLORO-5-ETHYL-6-METHYLTHIENO[2,3-D]PYRIMIDINE is used as a building block for the synthesis of various biologically active compounds due to its unique structure and pharmacological properties.
Used in Medicinal Chemistry and Drug Discovery:
4-CHLORO-5-ETHYL-6-METHYLTHIENO[2,3-D]PYRIMIDINE is utilized in the field of medicinal chemistry and drug discovery for its potential applications in developing new therapeutic agents.
Used in Herbicide Development:
4-CHLORO-5-ETHYL-6-METHYLTHIENO[2,3-D]PYRIMIDINE is investigated for its potential use as a herbicide due to its structural similarities to known herbicidal compounds, offering a promising avenue for the development of new agricultural chemicals.

InChI:InChI=1/C9H9ClN2S/c1-3-6-5(2)13-9-7(6)8(10)11-4-12-9/h4H,3H2,1-2H3

Upstream product

• 439692-89-4 5-ethyl-6-methylthieno[2,3-d]pyrimidin-4(3H)-one 
• 96-22-0 pentan-3-one 
• 4651-92-7 2‐amino‐4‐ethyl‐5‐methylthiophene‐3‐carbonitrile 
• 107-87-9 2-Pentanone 
• 82546-91-6 ethyl 2-amino-4-ethyl-5-methyl-thiophene-3-carboxylate 

Downstream Products

• 439692-91-8 C₉H₁₂N₄S 

Relevant academic research and scientific papers

Stimulation of cortical bone formation with thienopyrimidine based inhibitors of Notum Pectinacetylesterase

A group of small molecule thienopyrimidine inhibitors of Notum Pectinacetylesterase are described. We explored both 2-((5,6-thieno[2,3-d]pyrimidin-4-yl)thio)acetic acids and 2-((6,7-thieno[3,2-d]pyrimidin-4-yl)thio)acetic acids. In both series, highly potent, orally active Notum Pectinacetylesterase inhibitors were identified.

SUBSTITUTED 4-(SELENOPHEN-2(OR-3)-YLAMINO)PYRIMIDINE COMPOUNDS AND METHODS OF USE THEREOF

Selenophene compounds of formula (I) are described herein. In the compounds of Formula (I), ring A is a 6-membered aromatic fused ring, optionally containing one, two or three nitrogen atoms; a 5-membered heteroaromatic fused ring; or a mono- or bicyclic

Convenient and efficient synthesis of some novel fused thieno pyrimidines using gewald's reaction

Several functionalized thienopyrimidines were synthesized by a facile synthetic method, which includes Gewald's reaction, and were characterized by spectral and analytical data. These functionalized thienopyrimidines were converted to various new chemical

Discovery of novel thieno[2,3-d]pyrimidin-4-yl hydrazone-based inhibitors of Cyclin D1-CDK4: Synthesis, biological evaluation, and structure-activity relationships

The synthesis and evaluation of new analogues of thieno[2,3-d]pyrimidin-4-yl hydrazones are described. 2-Pyrdinecarboxaldehyde [6-(tert-butyl)thieno[2,3-d]pyrimidine-4-yl]hydrazone derivatives have been identified as cyclin-dependent kinase 4 (CDK4) inhibitors. The potency, selectivity profile, and structure-activity relationship of this series of compounds are discussed.