937367-26-5

Basic information

• Product Name: mono-tert-butoxycarbonyl-1,11-diaminoundecane
• Synonyms: mono-tert-butoxycarbonyl-1,11-diaminoundecane
• CAS NO: 937367-26-5
• Molecular Weight: 286.458
• Mol File: 937367-26-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: mono-tert-butoxycarbonyl-1,11-diaminoundecane(CAS DataBase Reference)
• NIST Chemistry Reference: mono-tert-butoxycarbonyl-1,11-diaminoundecane(937367-26-5)
• EPA Substance Registry System: mono-tert-butoxycarbonyl-1,11-diaminoundecane(937367-26-5)

Safety Data

• Hazardous Substances Data: 937367-26-5(Hazardous Substances Data)

Usage

Description

tert-Butyl (11-aminoundecyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Upstream product

• 822-08-2 1,11-diaminoundecane 
• 1538-75-6 2,2-dimethylpropanoic anhydride 
• 24424-99-5 di-tert-butyl dicarbonate 

Relevant articles and documents

IRAK DEGRADERS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same.

OXOBENZINDOLIZINOQUINOLINES AND USES THEREOF

The synthesis of aromathecins, substituted 12H-5,l la-diazadibenzo[b,h]fluoren- 11 -ones is described. Use of these cytotoxic compounds and pharmaceutical compositions containing them for the treatment of cancer is described. Two novel processes for the synthesis of this system and a series of 14-substituted aromathecins as novel cytotoxic, topoisomerase I poisons are described.

N-SUBSTITUTED INDENOISOQUINOLINES AND SYNTHESES THEREOF

N-Substituted indenoisoquinoline compounds, and pharmaceutical formulations of N-substituted indenoisoquinoline compounds are described. Also described are processes for preparing N-substituted indenoisoquinoline compounds. Also described are methods for