13120-03-1

Basic information

• Product Name: N,N-dimethylbenzenecarboselenoamide
• Synonyms: N,N-Dimethylselenobenzamide
• CAS NO: 13120-03-1
• Molecular Formula: C₉H₁₁NSe
• Molecular Weight: 212.1503
• Mol File: 13120-03-1.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 256.2°C at 760 mmHg
• Flash Point: 108.8°C
• Vapor Pressure: 0.0156mmHg at 25°C
• CAS DataBase Reference: N,N-dimethylbenzenecarboselenoamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethylbenzenecarboselenoamide(13120-03-1)
• EPA Substance Registry System: N,N-dimethylbenzenecarboselenoamide(13120-03-1)

Safety Data

• Hazardous Substances Data: 13120-03-1(Hazardous Substances Data)

Upstream product

• 100-47-0 benzonitrile 
• 124-40-3 dimethyl amine 
• 2397-26-4 N,N-dimethyl(chlorophenylmethylene)ammonium chloride 
• 611-74-5 N,N-dimethylbenzamide 
• 5395-11-9 dimorpholinodiselenane 
• 1080-32-6 O,O-diethyl benzylphosphonate 

Downstream Products

• 1072006-82-6 2-(N,N-dimethylamino)-2-phenyl-cyclopropanecarboxylic acid n-butyl ester 
• 87143-88-2 N,N-dimethyl-N-(1,3-diphenyl-2-propynyl)amine 
• 2371-23-5 1,2-diphenylhexan-1-one 
• 73475-28-2 N,N-dimethyl benzenecarbotelluroamide 
• 1009-14-9 phenyl butyl ketone 
• 5336-72-1 dimethyl(diphenylmethyl)amine 
• 33331-39-4 (Z)-N,N,N',N'-Tetramethyl-1,2-diphenyl-ethene-1,2-diamine 

Relevant articles and documents

Reaction of diisobutylaluminium hydride with selenium and tellurium: New reagents for the synthesis of seleno- and telluro-amides

Diisobutylaluminium hydride (BuI2AlH) undergoes reaction with elemental selenium and tellurium to afford new reagents having an Al-Se or an Al-Te bond. These directly convert amides to selenoamides and telluroformamides. This affords

3,4,5-Tris(2,4-di-t-butyl-6-methoxyphenyl)3,4,5-triselenoxo-1,2-diselena-3,4,5-triphospholane as a Selenation Reagent

A new type of phosphorus-selenium containing heterocyclic compound, 3,4,5-tris(2,4-di-t-butyl-6-methoxyphenyl)-3,4,5-triseleno-1,2-diselena-3,4,5-triphospholane, was prepared and was allowed to react with amides to give the corresponding selenoamides in g

Tertiary selenoamide compounds are useful superoxide radical scavengers in vitro

We investigated the scavenging effects of tertiary selenoamide compounds for super oxide radicals using a highly sensitive and quantitative chemiluminescence method. At 333 nM, tertiary selenoamide compounds scavenged 25.8-81.6% of O2-/su

Facile synthesis of N,N-dialkylselenoamides from amides

The synthesis of the N,N-dialkylselenoamides from amides was discussed. These selenoamides were chlorinated with oxalyl chloride and then they were allowed to react with LiAlHSeH to afford the corresponding N,N-dialkylamides in moderate to good yields. Af