41563-68-2

Upstream product

• 51689-51-1 (2-methyl-1,3-phenylene)dimethanol 
• 526-73-8 1,2,3-trimethylbenzene 
• 81-84-5 1,8-Naphthalic anhydride 
• 15120-47-5 2-methyl-1,3-benzenedicarbocylic acid 
• 855270-56-3 2-Methyl-isophthalsaeure-diaethylester 
• 54454-12-5 (3-chloro-2-methylphenyl)carbonitrile 
• 2317-22-8 2,6-dicyanotoluene 
• 3112-43-4 acide 2,6-carboxyphenylglyoxalique 
• 28269-31-0 dimethyl 2-methylbenzene-1,3-dicarboxylate 

Downstream Products

• 81649-89-0 anti-9-methyl-18-phenyl-2,11-dithia<3,3>metacyclophane 
• 126694-39-1 8-Methyl-N-(p-tolylsulfonyl)-1-thia-10-aza<2.2>metacyclophan 
• 120188-97-8 2-Methyl-1,3-bis-selenocyanatomethyl-benzene 
• 131298-24-3 17,17,18,18-Tetradehydro-8-methyl-1,10-bis(p-tolylsulfonyl)-1,10-diaza<2>(1,3)benzeno<2>(1,2)benzeno<2>(1,2)benzenophan 
• 41563-67-1 2-methyl-1,3-bis(mercaptomethyl)benzene 
• 89467-10-7 dibromure de 2,6-bis(triphenylphosphoniomethyl)toluene 
• 28746-25-0 2,6-Bis(methoxymethyl)toluol 
• 65276-20-2 2,3,2',3'-tetramethyl-bibenzyl 
• 28746-22-7 3-Brommethyl-2-methyl-benzyltriphenylphosphonium-bromid 
• 26787-71-3 anti-9,18-dimethyl-2,11-dithia<3,3>metacyclophane 
• 28746-27-2 3-(Methoxymethyl)-2-methylbenzaldehyde 
• 28746-26-1 3-Methoxymethyl-2-methylbenzaldehyd-dimethylacetal 
• 28817-09-6 3,3'-Bis(bromomethyl)-2-methyl-stilben 
• 28817-06-3 3,3'-Bis(bromomethyl)-2-methyl-trans-stilben 

Relevant academic research and scientific papers

Structural elucidation of an oxidation product of sedimentary porphyrins by one-pot synthesis of 3-methylphthalimide

One-pot synthesis of 3-methylphthalimide was achieved from 1,2,3-trimethylbenzene. The starting compound was oxidized in two steps to produce methylphthalic acids. The o-isomer was converted into its anhydride, which was subjected to thermal reaction with urea to form 3-methylphthalimide. The product was identical with the reported oxidation product of sedimentary porphyrins.

SYNTHESE PHOTOCHIMIQUE D'HYDROCARBURES POLYCYCLIQUES AROMATIQUES ET ETUDE EN RMN-1H DES PROTONS DE BAIE. EFFECTS DE SOLVANT SPECIFIQUES ET EFFECTS NUCLEAIRES OVERHAUSER.

"Photochemical synthesis of polycyclic aromatic hydrocarbons and NMR-1H study of bay protons.Specific solvent effects and nuclear Overhauser effects".Dinaphthoanthracene (4a),9-bromo-dinaphthoanthracene (4b), 9-methyldinaphthoanthracene (4c), benzonaphthochrysene (7), benzonaphthoanthracene (3), naphthochrysene (9) and dibenzonaphthochrysene (12) have been synthesized by the photocyclodehydrogenation of 1,2-diarylethylenes (5,8) and bis (arylvinyl)arenes (6,10).The NMR study has been mainly focused on the bay protons involved in specific solvent effects Table 4) and nuclear Overhauser effects (Table 5).