114552-32-8

Usage

Uses

Used in Pharmaceutical Industry:
(2-Trimethylstannanyl-phenyl)-carbamic acid tert-butyl ester is used as a synthetic intermediate for the production of pharmaceuticals. Its unique structure allows for the creation of a wide range of medicinal compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, (2-Trimethylstannanyl-phenyl)-carbamic acid tert-butyl ester is used as a precursor in the synthesis of various agrochemicals. Its reactivity and stability make it suitable for the development of effective and safe crop protection products.
Used in Organic Chemistry Research:
(2-Trimethylstannanyl-phenyl)-carbamic acid tert-butyl ester is used as a valuable tool in organic chemistry research. Its ability to participate in a variety of reactions makes it an essential component in the development of new synthetic methods and the exploration of novel chemical reactions.
Used in Fine Chemicals Production:
(2-TRIMETHYLSTANNANYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is also used in the production of fine chemicals, which are high-purity specialty chemicals used in various industries, including fragrances, flavors, and cosmetics. The versatility of (2-Trimethylstannanyl-phenyl)-carbamic acid tert-butyl ester contributes to the synthesis of high-quality fine chemicals with specific properties and applications.

Upstream product

• 3422-01-3 tert-butyl phenylcarbamate 
• 1066-45-1 trimethyltin(IV)chloride 
• 62-53-3 aniline 
• 7646-78-8 tin(IV) chloride 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 187219-43-8 5,8-dimethoxy-7-nitro-4-[2'-(tert-butoxycarbonylamino)phenyl]quinoline 
• 185408-19-9 2-(2-tert-Butoxycarbonylamino-phenyl)-5-(tert-butyl-dimethyl-silanyloxy)-5-((Z)-6-trimethylsilanyl-hex-3-ene-1,5-diynyl)-cyclohex-1-enecarboxylic acid methyl ester 
• 171725-33-0 2-(N'-Cbz-piperidine-4-carbonyl)-N-Boc-aniline 
• 180049-21-2 2,5-Bis(2'-tert-butylcarbonylaminophenyl)pyrazine 
• 305811-26-1 2-(2-aminophenyl)pyrazine 
• 866757-05-3 (3',5'-di-O-benzoyl-2'-deoxy-β-D-erythro-pentofuranosyl)-[2-(N-(tert-butoxycarbonyl)amino)phenyl] ketone 
• 866757-06-4 (3',5'-di-O-(p-toluoyl)-2'-deoxy-β-D-erythro-pentofuranosyl)-[2-(N-(tert-butoxycarbonyl)amino)phenyl] ketone 
• 1394920-36-5 o-(trimethylstannyl)aniline 
• 137039-31-7 2-<2-<(tert-Butoxycarbonyl)amino>phenyl>-5-hydroxy-1,4-naphthoquinone 
• 148493-41-8 [2-(2,6-Dichloro-pyridin-3-yl)-phenyl]-carbamic acid tert-butyl ester 
• 133400-99-4 6-bromo-5,8-dimethoxy-4-methylquinoline 
• 133400-98-3 6-bromo-4-<2-(tert-butoxycarbonyl)amino>-5,8-dimethoxyquinoline 
• 1440782-74-0 C₂₈H₃₇NO₄ 
• 117269-80-4 (S)-4-[2-(2-tert-Butoxycarbonylamino-phenyl)-2-oxo-ethyl]-5-oxo-oxazolidine-3-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

In-Cell Generation of Anticancer Phenanthridine Through Bioorthogonal Cyclization in Antitumor Prodrug Development

Pharmacological inactivation of antitumor drugs toward healthy cells is a critical factor in prodrug development. Typically, pharmaceutical chemists graft temporary moieties to existing antitumor drugs to reduce their pharmacological activity. Here, we re

O-(Trialkylstannyl)anilines and their utility in Migita-Kosugi-Stille cross-coupling: Direct introduction of the 2-aminophenyl substituent

We have developed shelf- and air-stable ortho-stannylated aniline reagents that can directly be coupled with alkenyl and aryl halides via Migita-Kosugi-Stille cross-coupling. We report (i) the efficient preparation of o-(tributylstannyl)aniline (2a) and o-(trimethylstannyl)aniline (2b), (ii) the comparison of the reactivities of 2a and 2b with those of related organostannanes in cross-coupling reaction with an alkenyl halide, and (iii) the cross-coupling of 2a and 2b with a series of arylhalides and triflate.