51694-16-7

Basic information

• Product Name: 1-methyl-3-selenocyanatobenzene
• Synonyms: 1-methyl-3-selenocyanatobenzene
• CAS NO: 51694-16-7
• Molecular Weight: 196.11
• Mol File: 51694-16-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-methyl-3-selenocyanatobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methyl-3-selenocyanatobenzene(51694-16-7)
• EPA Substance Registry System: 1-methyl-3-selenocyanatobenzene(51694-16-7)

Safety Data

• Hazardous Substances Data: 51694-16-7(Hazardous Substances Data)

Upstream product

• 2179-96-6 triselenium dicyanide 
• 17933-03-8 m-tolylboronic acid 
• 3425-46-5 potassium selenocyanate 
• 108-44-1 1-amino-3-methylbenzene 

Downstream Products

• 111090-23-4 biphenyl-4-yl-m-tolyl selenide 
• 69468-42-4 bis(3-methylphenyl) diselenide 
• 109286-48-8 m-tolyl-p-tolyl selenide 
• 1657-98-3 (2,4-dinitro-phenyl)-m-tolyl selenide 
• 172255-99-1 1-[(benzyloxy)methyl]-5-isopropyl-6-[(3-methylphenyl)selenenyl]-2-thiouracil 
• 172256-11-0 1-[(benzyloxy)methyl]-5-isopropyl-6-[(3-methylphenyl)selenenyl]uracil 
• 1026276-46-9 1-[2-(tert-Butyl-dimethyl-silanyloxy)-ethoxymethyl]-5-isopropyl-2-thioxo-6-m-tolylselanyl-2,3-dihydro-1H-pyrimidin-4-one 
• 1026694-92-7 1-[2-(tert-Butyl-dimethyl-silanyloxy)-ethoxymethyl]-5-isopropyl-6-m-tolylselanyl-1H-pyrimidine-2,4-dione 
• 1026372-53-1 1-[2-(tert-Butyl-dimethyl-silanyloxy)-ethoxymethyl]-5-ethyl-2-thioxo-6-m-tolylselanyl-2,3-dihydro-1H-pyrimidin-4-one 
• 1027145-79-4 1-[2-(tert-Butyl-dimethyl-silanyloxy)-ethoxymethyl]-5-ethyl-6-m-tolylselanyl-1H-pyrimidine-2,4-dione 
• 172255-78-6 5-ethyl-1-[(2-hydroxyethoxy)methyl]-6-[(3-methylphenyl)selenenyl]-2-thiouracil 
• 172255-84-4 5-ethyl-1-[(2-hydroxyethoxy)methyl]-6-[(3-methylphenyl)-selenenyl]uracil 
• 172255-90-2 1-(ethoxymethyl)-5-ethyl-6-[(3-methylphenyl)selenenyl]-2-thiouracil 
• 172255-81-1 1-[(2-hydroxyethoxy)methyl]-5-isopropyl-6-[(3-methylphenyl)-selenenyl]-2-thiouracil 

Relevant articles and documents

Metal-Free ipso -Selenocyanation of Arylboronic Acids Using Malononitrile and Selenium Dioxide

The first ipso -selenocyanation of arylboronic acids is achieved using selenium dioxide and malononitrile under mild conditions. The reaction is successful even without metal or base in DMSO. The major advantages of this new method are an easy set-up, excellent yields, and the use of odorless and inexpensive selenium reagents. Basic conditions subsequently afford new access to diaryldiselenides in good yields without isolating the organoselenocyanate intermediates.