164083-60-7

Basic information

• Product Name: tert-butyl 2,5-dimethylphenylcarbamate
• Synonyms: tert-butyl 2,5-dimethylphenylcarbamate
• CAS NO: 164083-60-7
• Molecular Formula: C₁₃H₁₉NO₂
• Molecular Weight: 221.29546
• Mol File: 164083-60-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: tert-butyl 2,5-dimethylphenylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 2,5-dimethylphenylcarbamate(164083-60-7)
• EPA Substance Registry System: tert-butyl 2,5-dimethylphenylcarbamate(164083-60-7)

Safety Data

• Hazardous Substances Data: 164083-60-7(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 95-78-3 2,5-Dimethylaniline 
• 24608-52-4 tert-butyl chloroformate 
• 4248-19-5 tert-butyl carbazate 
• 553-94-6 4-bromo-m-xylene 

Downstream Products

• 1250690-31-3 2,5-dimethyl-N-prop-2-yn-1-yl-benzenamine 

Relevant articles and documents

Organocatalytic Para-Selective Amination of Phenols with Iminoquinone Monoacetals

A highly selective para C-H amination of unprotected phenols with iminoquinone acetals was realized, giving the functional phenols in good to excellent yields. Overall, this transformation is operationally simple, proceeds with readily available phenols, and has wide substrate scope and low catalyst loading. The biarylamine product is stochastically formed via [5,5]-sigmatropic rearrangement of a mixed acetal species which is generated in situ under the reaction conditions.

Room-temperature Pd-catalyzed amidation of aryl bromides using tert-butyl carbamate

(Chemical Equation Presented) The scope of Pd-catalyzed synthesis of N-Boc-protected anilines from aryl bromides and commercially available tertbutyl carbamate is described. For the first time, this process can be conducted at room temperature (17-22°C) u