7020-81-7

Basic information

• Product Name: propylidene-t-butylamine
• Synonyms: propylidene-t-butylamine
• CAS NO: 7020-81-7
• Molecular Weight: 113.203
• Mol File: 7020-81-7.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: propylidene-t-butylamine(CAS DataBase Reference)
• NIST Chemistry Reference: propylidene-t-butylamine(7020-81-7)
• EPA Substance Registry System: propylidene-t-butylamine(7020-81-7)

Safety Data

• Hazardous Substances Data: 7020-81-7(Hazardous Substances Data)

Upstream product

• 123-38-6 propionaldehyde 
• 75-64-9 tert-butylamine 

Downstream Products

• 86783-39-3 tert-Butyl-[(Z)-2-(toluene-4-sulfinyl)-propenyl]-amine 
• 82483-91-8 tert-Butyl-[(Z)-2-((S)-toluene-4-sulfinyl)-propenyl]-amine 
• 25532-74-5 (+)-(S)-nuciferal 
• 111077-76-0 1-tert-butyl-3,5-dimethyl-2-phenyl-1,2-dihydro-1,2-λ³-azaphosphinine 
• 131270-31-0 1-tert-butyl-3-ethyl-4-methyl-2-phenyl-2-oxo-1,2,4-azaphospholene 
• 131270-50-3 1-tert-Butyl-4-methyl-2,3-diphenyl-1,3-dihydro-[1,2,3]azadiphosphole 2-oxide 
• 111077-85-1 1-tert-butyl-3,5-dimethyl-2-phenyl-2-thioxo-1,2-dihydro-1,2-azaphosphinine 
• 131270-51-4 1-tert-butyl-2,3-diphenyl-4-methyl-2-oxo-3-thioxo-1,2,3-azadiphospholene 
• 67467-96-3 2-methyl-3-(4-(tert-pentyl)phenyl)propanal 
• 1425046-82-7 2-methyl-N-(2-methyl-4-phenylbutylidene)propan-2-amine 
• 131270-48-9 1-tert-butyl-2-benzyl-3,5-dimethyl-2-oxo-1,2-dihydro-1,2-azaphosphinine 
• 137452-03-0 N-t-Butyl(2-p-tolylsulphinyl)propylamine 
• 137452-03-0 N-t-Butyl(2-p-tolylsulphinyl)propylamine 
• 137452-02-9 N-t-Butyl-2-(phenylsulphinyl)propylamine 

Relevant articles and documents

Synthesis of pyrrolizidines by cascade reactions of N- alkenylaziridinylmethyl radicals

Pyrrolizidines were synthesized in a one-step-reaction from 2- (bromomethyl)aziridines via a cascade of radical reactions involving aziridinylmethyl radicals. N-allylaminyl radicals and carbon-centered pyrrolidinyl radicals.

5-Benzylidene-4-oxazolidinones potently inhibit biofilm formation in Methicillin-resistant Staphylococcus aureus

Investigation into the biological function of 5-benzylidene-4-oxazolidinones revealed dose-dependent inhibition of biofilm formation in Methicillin-resistant S. aureus (MRSA). This structurally unusual class of small molecules inhibit up to 89% of biofilm formation with IC50 values as low as 0.78 μM, and disperse pre-formed biofilms with IC50 values as low as 4.7 μM. Together, these results suggest that 4-oxazolidinones represent new chemotypes to enable the study of bacterial biofilms with small molecule chemical probes.

NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS

The present application relates to isothiazolylidene containing compounds of Formula (I) wherein R1, R2, R3, R4, and L are as defined in the specification, compositions comprising such compounds, and methods for treating conditions and disorders using such compounds and compositions.