19715-31-2

Upstream product

• 19715-30-1 2,6-di-t-butyl-4-nitrobromobenzene 
• 740815-84-3 2-[2,5-dibromo-3-(1,1-dimethyl-2-oxo-ethyl)-phenyl]-2-methyl-propionaldehyde 
• 3975-77-7 1-bromo-2,4,6-tri-tert-butylbenzene 
• 5180-59-6 2,6-di-tert-butyl-4-nitro-aniline 
• 740815-83-2 2,5-dibromo-1,3-bis(1-cyano-1-methylethyl)benzene 
• 740815-80-9 2,5-dibromo-1,3-di-tert-butylbenzene 
• 19715-32-3 2-bromo-1,3-di-tert-butylbenzene 
• 740815-91-2 (4-bromo-3,5-di-tert-butylphenyl)(diphenylmethylene)amine 

Downstream Products

• 19715-32-3 2-bromo-1,3-di-tert-butylbenzene 
• 19715-33-4 2-bromo-1,3-di-tert-butyl-5-(dimethylamino)benzene 
• 127043-86-1 (1R,2R)-3,3-Dichloro-1,2-bis-(2,6-di-tert-butyl-phenyl)-diphosphirane 
• 19715-29-8 Bis-(4-Dimethylamino-2,6-di-tert.-butyl-phenyl)-disulfid 
• 19715-25-4 Bis-<2,6-di-tert.butyl-phenyl>-disulfid 
• 19728-49-5 4-Dimethylamino-2,6-di-tert.-butyl-thiophenol 
• 19728-46-2 2,6-di(tert-butyl)benzenethiol 
• 127043-86-1 (1R,2S)-3,3-Dichloro-1,2-bis-(2,6-di-tert-butyl-phenyl)-diphosphirane 
• 127043-87-2 1,3-bis(2,6-di-t-butylphenyl)-1,3-diphosphaallene 
• 127043-85-0 C₂₈H₄₂P₂ 
• 127043-84-9 2,6-di-t-butylphenylphosphonous dichloride 
• 127043-88-3 bis(4-bromo-3,5-di-t-butylphenyl) ether 

Relevant academic research and scientific papers

Preparation and properties of phosphaethynes bearing bulky aryl groups with electron-donating substituents at the para position

Phosphaethynes bearing a 2,6-di-tert-butyl-4-(dimethylamino)phenyl, 2,6-di-tert-butyl-4-methoxyphenyl, or 2,6-di-tert-butylphenyl group were prepared. A 31P NMR spectroscopic investigation of the chemical shifts indicated that electron-donating

SOME NEW PROTECTIVE GROUPS FOR STABILIZING LOW COORDINATED PHOSPHORUS COMPOUNDS

Sterically stabilized diphosphenes and 1,3-diphosphaallenes by 2,4-di-t-butylphenyl or 2,4,6-tri-t-pentylphenyl groups were prepared.

A VERSATILE PREPARATION OF 2,6-DI-t-BUTYLBROMOBENZENE. APPLICATION TO STERIC PROTECTION FOR ORGANOPHOSPHORUS COMPOUNDS IN LOW COORDINATION STATES

2,6-di-t-butylbromobenzene (5) was prepared from 2,4,6-tri-t-butyl-bromobenzene by ipso nitration followed by reduction of the nitro group and deamination.The diphosphene (8) and 1,3-diphosphaallene (10) were prepared.