85493-96-5

Upstream product

• 16807-60-6 3-methoxycyclohex-2-en-1-one 
• 504-02-9 1,3-cylohexanedione 
• 67-56-1 methanol 
• 52-90-4 L-Cysteine 
• 60060-44-8 2-bromocyclohexane-1,3-dienone 
• 18598-63-5 L-cysteine methyl ester hydrochloride 
• 72031-35-7 2-bromo-3-hydroxycyclohex-2-enone 
• 149-73-5 trimethyl orthoformate 
• 186581-53-3 diazomethane 

Downstream Products

• 221203-27-6 3-methoxy-2-vinyl-2-cyclohexenone 
• 94734-15-3 2-phenyl-3-methoxy-2-cyclohexenone 
• 92251-84-8 3-Methoxy-2-p-methoxyphenyl-cyclohex-2-en-1-on 
• 1231950-82-5 2-isopropyl-3,5,6,7-tetrahydro-4H-benzo[d]imidazol-4-one 
• 395642-61-2 2-bromo-3-ethenyl-2-cyclohexen-1-one 
• 1619228-46-4 2-bromo-3-(prop-1-en-2-yl)cyclohex-2-en-1-one 
• 395642-62-3 2-bromo-3-vinylcyclohex-2-en-1-ol 
• 1619228-48-6 2-bromo-3-(prop-1-en-2-yl)cyclohex-2-en-1-ol 
• 1619228-49-7 2-bromo-3-(prop-2-yn-1-yloxy)-1-vinylcyclohex-1-ene 
• 1619228-51-1 2-bromo-1-(prop-1-en-2-yl)-3-(prop-2-yn-1-yloxy)cyclohex-1-ene 
• 936226-23-2 2-bromo-3-methoxy-cyclohex-2-enone oxime 
• 87887-08-9 3-(2-bromo-3-oxocyclohex-1-enyl)hexahydro-1-methylazepin-2-one 

Relevant academic research and scientific papers

1H-IMIDAZO[4,5-H]QUINAZOLINE COMPOUND AS PROTEIN KINASE INHIBITOR

Provided is a 1H-imidazo[4,5-h]quinazoline compound of formula (I). The compound is a broad spectrum inhibitor having strong activity for cyclin-dependent kinase (CDK) and is applicable in treating cell proliferative disorder

IMINO COMPOUNDS AS PROTECTING AGENTS AGAINST ULTRAVIOLET RADIATIONS

The present invention relates to compounds having the general Formula I: which absorb UV radiations and protect biological materials as well as non-biological materials from damaging exposure to UV radiations. The present invention also relates to formulations and compositions comprising such compounds for use in absorbing UV radiations and in protecting biological materials as well as non-biological materials against UV radiations.

PROCESS FOR PREPARING SUBSTITUTED ANISIDINES

Disclosed is a process for preparing substituted anisidines of formula I starting from substituted cyclic hydroxy-ketones II via aromatization through a substituted oxime intermediate IV in which R is C1-C6 alkyl or halogen, and Alk is C1-C6 alkyl. The su

An efficient synthesis of 2-aryl and 2-alkenyl-3-alkoxy-cyclohexenones by a modified stille reaction

A general, direct procedure for the synthesis of 2-aryl and 2-alkenyl- 3-alkoxy-cyclohexenones using a modified Stille coupling is described.

2-Bromo-3-methoxycyclohex-2-enone, a New Reagent for the α-Arylation of Lactams

We report efficient syntheses of 2-bromo and 2-chloro-3-methoxycyclohex-2-enone and their use as m-hydroxyphenyl cation synthons for the α-arylation of lactams.The sequence has been used to synthesize the analgesic drug meptazinol.