955929-58-5

Basic information

• Product Name: 4-cyano-2,6-dimethylphenyl trifluoromethanesulfonate
• Synonyms: 4-cyano-2,6-dimethylphenyl trifluoromethanesulfonate
• CAS NO: 955929-58-5
• Molecular Weight: 279.24
• Mol File: 955929-58-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 4-cyano-2,6-dimethylphenyl trifluoromethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-cyano-2,6-dimethylphenyl trifluoromethanesulfonate(955929-58-5)
• EPA Substance Registry System: 4-cyano-2,6-dimethylphenyl trifluoromethanesulfonate(955929-58-5)

Safety Data

• Hazardous Substances Data: 955929-58-5(Hazardous Substances Data)

Upstream product

• 37595-74-7 N,N-phenylbistrifluoromethane-sulfonimide 
• 4198-90-7 3,5-dimethyl-4-hydroxybenzonitrile 
• 358-23-6 trifluoromethylsulfonic anhydride 

Downstream Products

• 1233244-42-2 4-allyl-3,5-dimethylbenzonitrile 
• 1233243-52-1 (E)-Methyl 3-(4-cyano-2,6-dimethylphenyl)acrylate 
• 90877-62-6 4-isopropyl-3,5-dimethylbenzonitrile 
• 1350824-26-8 3-{2,6-dimethyl-4-[5-(1-methyl-5-phenyl-1H-pyrazol-3-yl)-1,2,4-oxadiazol-3-yl]phenyl}propane-1,2-diol 
• 1350824-95-1 2-(2,6-dimethyl-4-(5-(1-methyl-5-phenyl-1H-pyrazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetaldehyde 
• 1350824-94-0 3-(4-allyl-3,5-dimethylphenyl)-5-(1-methyl-5-phenyl-1H-pyrazol-3-yl)-1,2,4-oxadiazole 
• 1233477-83-2 4-allyl-N'-hydroxy-3,5-dimethylbenzimidamide 
• 867367-02-0 4-fluoro-3,5-dimethylbenzonitrile 

Relevant articles and documents

Efficient cross-coupling of aryl/alkenyl triflates with acyclic secondary alkylboronic acids

Aryl-secondary alkyl cross-coupling with aryl sulfonate esters as coupling partners remains a significant challenge. Efficient cross-coupling between aryl/alkenyl triflates and acyclic secondary alkylboronic acids is realized for the first time to provide a series of sterically congested acyclic secondary alkyl arenes/olefins in good to excellent yields. The employment of sterically bulky P,PO ligand L1/L2 is crucial for the high yields and selectivities. The method has enabled a concise and 4-step synthesis of a key intermediate of male contraceptive agent and PAF antagonist gossypol.

NEW OXADIAZOLE DERIVATIVES

The present invention relates to an oxadiazole derivative of formula (I)1 or a pharmaceutically acceptable salt or N-oxide thereof: wherein, R1 represents a hydrogen atom, a C1-2 alkyl group or a C3-4 cycloalkyl-C1-2

New pyrazole derivatives

The present invention relates to a compound of formula (I), to the process for preparing such compounds and to their use in the treatment of a pathological condition or disease susceptible to amelioration by sphingosine-1-phosphate receptors (S1P1) agonists.