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| 1,5-bis-Boc-1,5,10-triazadecane Basic information |
| Product Name: | 1,5-bis-Boc-1,5,10-triazadecane | | Synonyms: | 1,5-bis-Boc-1,5,10-triazadecane;N1,N4-bis-Boc-sperMidine;N1,N4-Bis-Boc-spermidine >=95.0% (TLC);N-(4-aminobutyl)-N-[3-[[(1,1-dimethylethoxy)carbonyl]amino]propyl]Carbamic acid 1,1-dimethylethyl ester;tert-butyl N-(4-aminobutyl)-N-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]carbamate;Carbamic acid, N-(4-aminobutyl)-N-[3-[[(1,1-dimethylethoxy)carbonyl]amino]propyl]-, 1,1-dimethylethyl ester;N1,N4-Bis-spermidine;tert-butyl (4-aminobutyl)(3-((tert-butoxycarbonyl)amino)propyl)carbamate | | CAS: | 85503-20-4 | | MF: | C17H35N3O4 | | MW: | 345.48 | | EINECS: | | Product Categories: | | Mol File: | 85503-20-4.mol |
| 1,5-bis-Boc-1,5,10-triazadecane Chemical Properties |
| storage temp. | -20°C | | BRN | 6418809 |
| 1,5-bis-Boc-1,5,10-triazadecane Usage And Synthesis |
| Description | 1,5-Bis-Boc-1,5,10-triazadecane is a linker containing an amino group with two Boc-protected amino groups. The amino 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. | | Uses | N1,N4-Bis-Boc-spermidine is an antibiotic enhancers against resistant gram-negative bacteria and it is an anticancer agent. |
| 1,5-bis-Boc-1,5,10-triazadecane Preparation Products And Raw materials |
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