103234-38-4

Usage

InChI:InChI=1/C13H16O4/c1-8-6-10(7-9(2)13(8)17-3)11(14)4-5-12(15)16/h6-7H,4-5H2,1-3H3,(H,15,16)

Upstream product

• 108-30-5 succinic acid anhydride 
• 1004-66-6 2-methoxy-1,3-dimethylbenzene 

Downstream Products

• 52246-10-3 4-(4-hydroxy-3,5-dimethylphenyl)-4-oxobutyric acid methyl ester 
• 948995-57-1 4-[3,5-dimethyl-4-(4-nitro-benzyloxy)-phenyl]-4-oxo-butyric acid methyl ester 
• 948995-77-5 C₅₂H₆₅N₅O₂₄ 
• 948995-75-3 C₄₀H₄₉N₅O₁₆ 
• 948995-63-9 N-[2-(2-azidoethoxy)ethyl]-4-[3,5-dimethyl-4-(4-nitrobenzyloxy)phenyl]-4-oxobutyramide 

Relevant academic research and scientific papers

Design, Conformation, and Crystallography of 2-Naphthyl Phenyl Ethers as Potent Anti-HIV Agents

Catechol diethers that incorporate a 7-cyano-2-naphthyl substituent are reported as non-nucleoside inhibitors of HIV-1 reverse transcriptase (NNRTIs). Many of the compounds have 1-10 nM potencies toward wild-type HIV-1. An interesting conformational effect allows two unique conformers for the naphthyl group in complexes with HIV-RT. X-ray crystal structures for 4a and 4f illustrate the alternatives.

Photocleavable molecule for laser desorption ionization mass spectrometry

(Figure Presented) A new photocleavable molecule for laser desorption ionization mass spectrometry (LDI-MS) was designed and synthesized. The molecule exhibited high sensitivity for negative mode MS detection with good chemical stability. The molecule was successfully applied to molecular tag for (LDI-MS). Kinetic measurement of the amidation reaction and monitoring of aminolysis of acetylated sugars were demonstrated with the molecular tag.

Herbicidal cyclohexane-1,3-dione derivatives

The invention concerns novel compounds of the formula I and isomers thereof STR1 wherein: n is an integer selected from 2 to 4; m is zero or an integer selected from 1 to 3; X, which may be the same or different, are independently selected from halogen, a