N-Boc-undecane-1,11-diamine

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Company Name: Nextpeptide Inc
Tel: +86-0571-81612335 +8613336028439
Email: sales@nextpeptide.com
Products Intro: Product Name:N-Boc-undecane-1,11-diamine
CAS:937367-26-5
Purity:98% Min. Package:5KG;1KG
Company Name: Sichuan Biosynce Pharmatech Co., Ltd.
Tel: +8619950309693
Email: diane@biosynce.com
Products Intro: Product Name:tert-Butyl (11-aminoundecyl)carbamate
CAS:937367-26-5
Purity:0.95_) Package:100G;500G;1KG Remarks:Chemically Pure
Company Name: Jilin Chinese Academy of Sciences-yanshen Technology
Tel: +undefined18143011203
Email: info@chemextension.com
Products Intro: Product Name:tert-Butyl (11-aminoundecyl)carbamate
CAS:937367-26-5
Purity:95%+ Package:1g;5g;10g;25g;50g;100g; Remarks:accept Custom Synthesis Services, support large packing
Company Name: Suzhou ARTK Medchem Co., Ltd.
Tel: +8618168183658
Email: sales1@artkmedchem.com
Products Intro: Product Name:tert-butylN-(11-aminoundecyl)carbamate
CAS:937367-26-5
Purity:0.98 Package:100KG;25KG;10KG;1KG
Company Name: PharmaBlock Sciences (Nanjing),Inc.  
Tel: 400-0255188 4000255188
Email: sales@pharmablock.com
Products Intro: Product Name:tert-butyl N-(11-aminoundecyl)carbamate
CAS:937367-26-5
Purity:97% Package:1G;5G;10G;100G;250G
N-Boc-undecane-1,11-diamine Basic information
Product Name:N-Boc-undecane-1,11-diamine
Synonyms:tert-Butyl (11-aminoundecyl)carbamate;Carbamic acid, N-(11-aminoundecyl)-, 1,1-dimethylethyl ester;N-Boc-undecane-1,11-diamine;N1-Boc-undecane-1,11-diamine;tert-butyl N-(11-aminoundecyl)carbamate
CAS:937367-26-5
MF:C16H34N2O2
MW:286.45
EINECS:
Product Categories:
Mol File:937367-26-5.mol
N-Boc-undecane-1,11-diamine Structure
N-Boc-undecane-1,11-diamine Chemical Properties
Safety Information
MSDS Information
N-Boc-undecane-1,11-diamine Usage And Synthesis
Descriptiontert-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.
N-Boc-undecane-1,11-diamine Preparation Products And Raw materials
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